Fluorinated integrin antagonists

ABSTRACT

The present invention relates to fluorinated compounds of formula I and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing the fluorinated compounds of the invention, and methods of treating macular degeneration, diabetic retinopathy (DR), macular edema, diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO), by administering these compounds and pharmaceutical compositions to subjects in need thereof.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. Ser. No. 15/343,823 (nowallowed), filed on Nov. 4, 2016, which is a continuation of U.S. Ser.No. 14/766,322, filed on Aug. 6, 2015 (now U.S. Pat. No. 9,518,053),which is a U.S. National Phase application of International ApplicationNo. PCT/US2014/015372, filed on Feb. 7, 2014, which claims priority toand the benefit of U.S. Ser. No. 61/762,087, filed on Feb. 7, 2013, andU.S. Ser. No. 61/900,706, filed on Nov. 6, 2013, the contents of each ofwhich are incorporated herein by reference in their entireties.

BACKGROUND OF THE INVENTION

Age-related macular degeneration (AMD) is the leading cause of blindnessin people over the age of 55; and diabetic retinopathy (DR) is theleading cause in people under 55 (Klein, 1994; Williams, 2004). Bothdiseases are characterized by new blood vessel growth—choriodalneovascularization in AMD and retinal neovascularization in DR (Freund,1993; Speicher, 2003; Zarbin, 2004). Macular edema occurs when fluid andprotein deposits collect on or under the macula of the eye (a yellowcentral area of the retina) and cause it to thicken and swell (edema).Diabetic macular edema (DME) is similarly caused by leaking macularcapillaries. DME is the most common cause of visual loss in bothproliferative and non-proliferative DR. Thrombosis of central retinalvein (CRV) and its branches is the second most prevalent vascularpathology after DR, and results in abrupt decrease in visual acuity andis accompanied by macular edema. Thus, anti-angiogenesis treatments areuseful in combating all these conditions.

αv integrins have been shown to be involved in ocular angiogenesis.Expression of αv integrins is upregulated in various diseases orconditions, such as AMD and DR, and in mouse model of oxygen-inducedretinopathy (OIR) or retinopathy of prematurity (ROP) model (Takagi,2002). Also, αvβ3 is expressed in new vessels after photocoagulation,but not in normal choroidal vessels, in the laser-induced choroidalneovascularization model for AMD (Kamizuru, 2001). Administration of αvintegrins antagonists, such as a cyclic RGD peptide, has been shown toinhibit retinal and choroidal neovascularization (Friedlander, 1996;Chavakis, 2002; Luna, 1996; Riecke, 2001; Yasukawa, 2004).

Angiogenesis inhibitors targeting vascular endothelial growth factor(VEGF), other growth factors (e.g., fibroblast growth factor (FGF),platelet-derived growth factor (PDGF)), chemokines (e.g., IL8, SDF1,G-CSF), receptors (e.g., CXCR1, FGF-R, PLGFR, PDGFR, Tie-receptors),intracellular mediators (e.g., c-kit kinase, PI3 kinase, PKC), andextracellular mediators (e.g., integrins, cadherins), as well asinhibitors of pro-angiogenic targets (e.g., phosphoinositide 3 kinase),have been investigated for the treatment of AMD and DR. However,application of these drugs is limited due to various concerns, such astoxicity and complexity of administration. Further, αv integrinsinhibitors tested or currently in clinical trials for treating AMD andDR are not being successfully developed due to poor ocularpharmacokinetics and/or high levels of excipient/carrier (e.g.,benzalconium chloride and mannitol) known to cause damage to the eye.

Thus, there continues to be a need for improved compounds, compositions,and methods for treating AMD, DR, DME, and macular edema followingretinal vein occlusion, that are safe, effective, and convenientlyadministered. The present invention addresses the need.

SUMMARY OF THE INVENTION

The present invention provides novel fluorinated compounds which are αvintegrin antagonists, having formula I:

or a pharmaceutically acceptable salt or solvate thereof.

The present invention provides a pharmaceutical composition comprising acompound of the invention or a pharmaceutically acceptable salt orsolvate thereof, and a pharmaceutically acceptable carrier or excipient.

The present invention also provides a pharmaceutical compositioncomprising a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof, and a pharmaceutically acceptable carrier orexcipient, and further an active ingredient selected from the groupconsisting of a) an antagonist of integrin α5β1, b) acytotoxic/antiproliferative agent, c) an inhibitor of epidermal-derived,fibroblast-derived, or platelet-derived growth factor, d) an inhibitorof VEGF, e) an inhibitor of Flk-1/KDR, Flt-1, Tck/Tie-2, or Tic-1, andf) an inhibitor of phosphoinositide 3-kinase, and a mixture thereof.

The present invention further provides a pharmaceutical compositioncomprising a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof, and a pharmaceutically acceptable carrier orexcipient, and further an active ingredient selected from the groupconsisting of a) an antagonist of integrin α5β1, b) acytotoxic/antiproliferative agent, c) an inhibitor of epidermal-derived,fibroblast-derived, or platelet-derived growth factors, d) an inhibitorof VEGF, and e) an inhibitor of phosphoinositide 3-kinase, and a mixturethereof.

The present invention provides a method of treating or preventing adisease or condition in a subject, comprising administering to a subjectin need thereof a therapeutically effective amount of a compound of theinvention or a pharmaceutically acceptable salt or solvate thereof or atherapeutically effective amount of a pharmaceutical composition of theinvention. In one aspect, the invention provides treating a disease orcondition. In one aspect, the invention provides preventing a disease orcondition. In one aspect, the compound or pharmaceutical composition ofthe invention is administered topically.

The present invention provides a method of treating or preventing adisease or condition mediated by an αv integrin in a subject, comprisingadministering to a subject in need thereof a therapeutically effectiveamount of a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof or a therapeutically effective amount of apharmaceutical composition of the invention. In one aspect, the diseaseor condition is a disease or condition in which angiogenesis isinvolved. In a further aspect, the disease or condition is a disease orcondition in which ocular angiogenesis is involved.

The present invention also provides a method of treating or preventingan αvβ3 and/or αvβ5 integrin-mediated disease or condition in a subject,comprising administering to a subject in need thereof a therapeuticallyeffective amount of a compound of the invention or a pharmaceuticallyacceptable salt or solvate thereof or a therapeutically effective amountof a pharmaceutical composition of the invention. In one aspect, thedisease or condition is a disease or condition in which ocularangiogenesis is involved. In one aspect, the disease or condition ismacular degeneration. In one aspect, the disease or condition isage-related macular degeneration (AMD). In one aspect, the disease orcondition is diabetic retinopathy (DR). In one aspect, the disease orcondition is diabetic macular edema (DME). In one aspect, the disease orcondition is macular edema following retinal vein occlusion (RVO).

The present invention further provides a method of treating orpreventing AMD, DR, DME, or macular edema following RVO, comprisingadministering to a subject in need thereof, a therapeutically effectiveamount of a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof or a therapeutically effective amount of apharmaceutical composition of the invention. In one aspect, theinvention provides treating AMD, DR, DME, or macular edema followingRVO. In one aspect, the invention provides preventing AMD, DR, DME, ormacular edema following RVO.

The present invention further provides a method of treating orpreventing a disease or condition in a subject, comprising administeringto a subject in need thereof a therapeutically effective amount of acompound of the invention or a pharmaceutically acceptable salt orsolvate thereof or a therapeutically effective amount of apharmaceutical composition of the invention, in combination with one ormore therapies for treating or preventing the disease or condition. Inone aspect, the disease or condition is mediated by an αv integrin. In afurther aspect, the disease or condition is mediated by an αvβ3 and/orαvβ5 integrin. In one aspect, the disease or condition is a disease orcondition in which angiogenesis is involved. In a further aspect, thedisease or condition is a disease or condition in which ocularangiogenesis is involved. In one aspect, the therapy is an anti-VEGFtherapy. In a further aspect, the anti-VEGF therapy is intravitreallyinjected.

The present invention provides the use of a compound of the invention ora pharmaceutically acceptable salt or solvate thereof in treating orpreventing a disease or condition in a subject. In one aspect, the useis for treating a disease or condition. In one aspect, the use is forpreventing a disease or condition. In one aspect, the compound orpharmaceutical composition of the invention is formulated for use intopical administration.

The present invention provides the use of a compound of the invention ora pharmaceutically acceptable salt or solvate thereof in the manufactureof a medicament for the treatment or prevention of a disease orcondition in a subject. In one aspect, the invention provides for thetreatment of a disease or condition. In one aspect, the inventionprovides for the prevention of a disease or condition. In one aspect,the medicament is formulated for topical administration.

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention belongs. In the case of conflict, thepresent specification, including definitions, will control. In thespecification, the singular forms also include the plural unless thecontext clearly dictates otherwise. Although methods and materialssimilar or equivalent to those described herein can be used in thepractice or testing of the present invention, suitable methods andmaterials are described below. All publications, patent applications,patents, and other references mentioned herein are incorporated byreference. The references cited herein are not admitted to be prior artto the claimed invention. In addition, the materials, methods, andexamples are illustrative only and are not intended to be limiting.

Other features and advantages of the invention will be apparent from thefollowing detailed description and claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. A bar graph showing blood vessel counts (score) in the chick CAMassay

FIG. 2. A bar graph showing plasma and ocular distribution of CompoundA1 in rabbit

FIG. 3. A bar graph showing plasma and ocular distribution of CompoundA2 in rabbit

FIG. 4. A bar graph showing plasma and ocular distribution of CompoundA3 in rabbit

FIG. 5. Representative Fluorescein Angiography (FA) images of the eye onday 35 in animals following twice daily topical administration of (A) 50μL Compound A1, (B) 50 μL Compound A2, (C) 50 μL vehicle

DETAILED DESCRIPTION OF THE INVENTION

It is believed that a wide variety of diseases and conditions can betreated or prevented by inhibiting processes mediated by αv integrins.Thus, αv integrin antagonists represent a useful class of drugs fortreating or preventing those diseases and conditions. Integrins areheterodimeric transmembrane proteins through which cells attach andcommunicate with extracellular matrices and other cells. The αvintegrins are key receptors involved in mediating cell migration andangiogenesis. Antagonists of the integrins αvβ3 and αvβ5 are useful fortreating and preventing bone resorption, osteoporosis, vascularrestenosis, diabetic retinopathy, macular degeneration, angiogenesis,atherosclerosis, inflammation, viral disease, tumor growth, andmetastasis.

αv integrins have also been found to be involved in ocular angiogenesis,a process that can lead to various ocular diseases, such as age-relatedmacular degeneration (AMD), diabetic retinopathy (DR), diabetic macularedema (DME), and macular edema following retinal vein occlusion (RVO)(Freund, 1993; Speicher, 2003; Zarbin, 2004). Pro-angiogenic growthfactors, including VEGF and FGF, are up-regulated in AMD and DR, which,in turn, stimulate αv integrin expression. In the well-established mousemodel of oxygen-induced retinopathy (OIR) or retinopathy of prematurity(ROP) model, αv integrins and the ligand osteopontin are overexpressedin neovascular endothelial cells during the peak time of retinal vesselgrowth (Takagi, 2002). Cyclic peptides mimicking thearginine-glycine-asparagine (RGD) binding motif, through which αvintegrins bind to their extracellular matrix ligands, have been shown toinhibit retinal neo-vascularization in the mouse OIR model via variousroutes of administration (e.g., subcutaneous, intraperitoneal,periocular, or topical) (Friedlander, 1996; Chavakis, 2002; Luna, 1996;Riecke, 2001). Also, in the laser-induced choroidal neovascularizationmodel (rats), a well-accepted model for AMD, integrins αvβ3 and vonWillebrand factor are expressed on endothelial cells of new vesselsafter photocoagulation, but not in normal choroidal vessels (Kamizuru,2001). In this model, intravitreal injection of a cyclic RGD peptidesignificantly reduces the development of choroidal neovascularization(Yasukawa, 2004). In humans, expression of αvβ3 and αvβ5, which are notexpressed in normal retinal tissue, is observed in vascular cells in theeyes of DR patients (Friedlander, 1996; Luna, 1996), and high levels ofαvβ5 expression is primarily observed in ocular tissues in AMD patients(Friedlander, 1996).

Diseases or conditions of the retina (which is located at the back ofthe eye), including macular degeneration, DR, DME, and macular edemafollowing RVO, are very difficult to treat by systemic administration(e.g., oral, intravenous, intra-nasally, or inhalation) because theretina is difficult to access from the systemic circulation due to theblood-retinal barrier. Therefore, currently approved treatments (e.g.,anti-VEGF proteins or a chemically-modified anti-VEGF aptamer) formacular degeneration, DME, and macular edema following RVO must berepeatedly administered by intra-ocular injection (intravitrealadministration).

Many angiogenesis inhibitors targeting vascular endothelial growthfactor (VEGF) (e.g., the VEGF aptamer, pegaptanib, and the VEGF or VEGFreceptor (VEGFR)-targeted monoclonal antibodies, bevacizumab,ranibizumab, aflibercept) have been investigated for the treatment ofAMD and DR. However, only pegatanib, ranibizumab, aflibercept areapproved by the Food and Drug Administration. Further, all theVEGF-targeted drugs must be administered by intravitreal injection totreat AMD or DR. Intravitreal injection requires adequate anesthesia anda broad-spectrum microbicide, and the insertion of a syringe needle intothe eye using aseptic conditions, thus necessitating the administrationto be performed in a physician's office. For example, the dosage andadministration section of the ranibizumab Package Insert describes thecomplex requirements for administering the drug in a safe and effectivemanner: all of the ranibizumab vial contents are withdrawn through a5-micron, 19-gauge filter needle attached to a 1-cc tuberculin syringeunder aseptic technique; the filter needle should be discarded afterwithdrawal of the vial contents and should be replaced with a sterile30-gauge×½-inch needle for the intravitreal injection; the contentsshould be expelled until the plunger tip is aligned with the line thatmarks 0.05 mL on the syringe; the intravitreal injection procedureshould be carried out under controlled aseptic conditions (e.g., usingsterile gloves, a sterile drape, and a sterile eyelid speculum).

In addition to the practical limitations and strictures related to theneed for intravitreal injection in the treatment of ocular diseases,VEGF-targeted drugs only address VEGF-promoted angiogenesis, but notangiogenesis promoted by other growth factors, including fibroblastgrowth factor (FGF), and platelet-derived growth factor (PDGF).Targeting angiogenic molecules other than, or in addition to VEGF, mayreveal more effective and safer inhibitors of intraocularneovascularisation. Potential targets include growth factors (e.g.,angiopoietin, FGF, HGF, IGF-1, PDGF-B, PLGF), chemokines (e.g., IL8,SDF1, G-CSF), receptors (e.g., CXCR1, FGF-R, PLGFR, PDGFR,Tie-receptors), intracellular mediators (e.g., c-kit kinase, PI3 kinase,PKC), and extracellular mediators (e.g., integrins, cadherins). Severaldrugs which do not selectively target VEGF have indeed shownanti-angiogenic efficacy in eyes: Pazopanib (which blocks PDGFRs, c-Kit,FGFR, and c-fms) suppresses choroidal neovascularization in mousemodels; and PKC412 (which blocks PKC, VEGF-R, PDGF-R and SCF-R isoforms)reduces macular oedema in diabetics (Doukas, 2008; Takahashi, 2009;Campochiara, 2004). Treatments that combine the action of theVEGF-targeted therapies with inhibition of one of these other growthfactors have also been studied. For example, a Phase 3 clinical trial isunderway testing the combination of ranibizumab and the anti-PDGFantibody designed E10030 (ClinTrials.gov, NCT01944839). However, thesetherapies are limited by safety concerns and complexity ofadministration, such as liver toxicity observed following oraladministration of PKC412, and intravitreal administration of ranibizumaband E10030.

Another approach for treating or preventing ocular diseases is toselectively target a distinct pro-angiogenic target, such as PI3K. Abroad-spectrum PI3K inhibitor LY294002 suppresses retinal or choroidalneovascularisation following intraocular injection in rodents (Yang,2009). Additional alternative treatments for AMD and DR involvingintravitreal administration of several small molecule inhibitors whichprevent angiogenesis (e.g., fibronectin receptor antagonists, JSM6427(Clin Trials.gov, NCT00536016) and ATN-161 (Wang, 2011), vascularendothelial protein tyrosine phosphatase inhibitors (ClinTrials.gov,NCT01702441), and mTOR inhibitors, sirolimus, and Palomar 529 (Jacot,2011)) are being tested in animals or in clinical trials. Further,combination therapies involving multiple foci of pro-angiogenic pathwayswith several selective inhibitors (e.g., combining angiostatic therapywith a VEGF aptamer, an integrin antagonist, and a proteolytic fragmentof tryptophan tRNA synthetase) have been shown to inhibit ocularangiogenesis (Dorrell, 2007). Despite these studies and clinical trials,no therapy with a favorable efficacy and safety profile has beenreported.

Recent advances in drug delivery technology, including formulation,polymer chemistry, nanotechnology, microdrug devices, and surgicaladvancements, have offered new options and opportunities for topicalocular drug administration. These technologies include the use ofhydrogels, mucoadhesive polymers, cyclodextrins, nanocompositeformulations, micellar and lipid nanoparticles, niosomes, microemulsion,microspheres, and prodrug derivatization. For instance, nanocompositeshave been used to deliver Diclofenac (Cao, 2011), and topicaladministration of Nepafenac has been shown to reduce the extent ofmicroangiopathy in animal models of DR (Kern, 2007) and oxygen-inducedretinopathy (Yanni, 2010). Also, nanoparticle technology has beenemployed to enhance the surface penetration of hydrophobic compoundssuch as glucocorticoids to posterior ocular structures (Diebold, 2010),and injection of nanoparticles into the vitreous has demonstratedintraretinal localization for several months after initial dosing andtherefore can be used as a localized drug release depot (Bourges, 2003).Topical administration using eye drops (e.g., eye drop formulationcomprising TG100572, which inhibits FGF, PDGF and VEGF (Doukas, 2008),or tyrosine kinase inhibitors (TKIs) (e.g., sorafenib (WO2013/000909),bradykinin receptor antagonists (ClinTrials.gov, NCT01319487), or ananti-microbial agent, squalamine (ClinTrials.gov, NCT01678963)) has beenstudied or is under investigation. However, none of these approacheshave been shown to be suitable for replacing the current standardanti-VEGF treatments that require intravitreal injection.

Oral or topical administration of drugs that inhibit αv integrins (e.g.,cyclic penta-peptide inhibitor of αvβ3 and αvβ5, cyclo-RGDfV,cilengetide, and the non-peptide αvβ3 and αvβ5 antagonist, JNJ-26076713and EMD478761), for example, by means of a polyvinyl alcohol-basedreservoir implant, has been tested or is currently in clinical trialsfor treating AMD and DR (Friedlander, 1996; Santulli, 2008; Fu, 2007).Cyclo-RGDfV was also tested in a mouse model of retinopathy ofprematurity administered by topical administration (Riecke, 2000);however, the compound needed to be administered six times a day, due tothe poor ocular pharmacokinetics of the compound (i.e., the amount ofthe compound that distributes to the retina after administration as eyedrops, and then maintains an adequate retinal concentration betweenadministrations). In addition, the peptide was formulated with highlevels of benzalconium chloride and mannitol, which are known to causedamage to the eye. As a result, topical administration has not beensuccessfully developed. To date, the most recent approach to treatingocular angiogenesis is through intravitreal injection of ALG-1001 (asynthetic oligo-peptide inhibitor of αvβ3, αvβ5, and α5β1), which cannotbe administered topically.

The present invention relates to novel fluorinated compounds, which areantagonists of the αv integrins, particularly integrins αvβ3 and/orαvβ5. The compounds of the present invention or pharmaceuticallyacceptable salts or solvates thereof are useful in treating orpreventing bone resorption, osteoporosis, vascular restenosis,atherosclerosis, inflammation, viral disease, tumor growth, ormetastasis. In particular, the compounds of the present invention orpharmaceutically acceptable salts or solvates thereof and pharmaceuticalcomposition comprising the compounds are effective in treating maculardegeneration, DR, DME, and macular edema following retinal veinocclusion (RVO) when administered topically.

Prior attempts to use small molecule integrin antagonists by topicaladministration have not succeeded because those compounds lack theappropriate physiochemical properties (e.g., lipophilicity, molecularsize and polar surface area) to allow delivery of therapeuticallyeffective amounts of those compounds by a convenient formulation anddosing regimen. The compounds of the present invention have beensurprisingly shown to distribute to the retina after topicaladministration in therapeutically effective amounts to inhibit thefunction of integrins αvβ3 and αvβ5 and thus treat or prevent retinalangiogenesis. The compounds of the present invention have advantagessuch as providing improved potency, selectivity, tissue penetration,half-life, and/or metabolic stability, and successful distribution tothe retina in therapeutically effective amounts via convenient topicaladministration to the eyes.

Compounds of the Invention

The present invention relates to novel fluorinated compounds of formulaI:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

Z is

R and R′ are each independently H or F, or R and R′, together with thecarbon atom to which they are attached, form a 3- or 4-memberedcarbocyclic or heterocyclic ring;

Q is

X is CH or N;

Y is CH or N;

R₁ is C₁-C₄ alkyl substituted with 1, 2, 3, 4, 5, 6, 7, 8, or 9 fluorineatoms, or C₁-C₆ alkoxy substituted with 0, 1, 2, 3, 4, 5, 6, or 7fluorine atoms; and

R₂ and R₃ are each independently H, F, CH₂F, CHF₂, or CF₃, provided thatone of R₂ and R₃ is not H,

provided that the compound of formula (I) contains at least one fluorineatom.

The compounds of the present invention contain at least one fluorineatom. In one aspect, the compounds of the present invention contain atleast one fluorine atom in the R or R′ substituent. In another aspect,the compounds of the present invention contain at least one fluorineatom in the R₁ substituent. In another aspect, the compounds of thepresent invention contain at least one fluorine atom in the R₂ or R₃substituent. Fluorination at any particular position, such as thatpresent in the compounds of the invention, has not been taught orsuggested.

In one aspect, Z is

In another aspect, Z is

In one aspect, R and R′ are each H. In another aspect, R and R′ are eachF. In another aspect, R is H and R′ is F.

In another aspect, R and R′, together with the carbon atom to which theyare attached, form a 3- or 4-membered carbocyclic or heterocyclic ring.In a further aspect, R and R′, together with the carbon atom to whichthey are attached, form a 4-membered heterocyclic ring. In a furtherembodiment, the 4-membered heterocyclic ring is an oxetane ring. Forexample, the oxetane ring is an oxetan-3-yl ring or oxetan-2-yl ring.

In one aspect, Q is

In one aspect, X is N and Y is CH. In another aspect, X and Y are eachCH. In another aspect, X and Y are each N.

In one aspect, R₁ is straight chain C₁-C₄ or branched C₃-C₄ alkyl, andis substituted with 1, 2, 3, 4, 5, 6, 7, 8, or 9 fluorine atoms. In afurther aspect, R₁ is methyl, ethyl, propyl, or butyl, and issubstituted with 1, 2, 3, 4, 5, 6, 7, 8, or 9 fluorine atoms. In afurther aspect, R₁ is methyl substituted with 1, 2, or 3 fluorine atoms.In a further aspect, R₁ is CF₃.

In another aspect, R₁ is straight chain C₁-C₆ or branched C₃-C₆ alkoxy,and is substituted with 0, 1, 2, 3, 4, 5, 6, or 7 fluorine atoms. In afurther aspect, R₁ is methoxy, ethoxy, propoxy, or butoxy, and issubstituted with 0, 1, 2, 3, 4, 5, 6, or 7 fluorine atoms. In a furtheraspect, R₁ is methoxy substituted with 0, 1, 2, or 3 fluorine atoms. Ina further aspect, R₁ is OCH₃, OCH₂F, OCHF₂, or OCF₃. In a furtheraspect, R₁ is OCHF₂.

In another aspect, Q is

In one aspect, R₂ is F. In a further aspect, R₂ is F and R₃ is H. Inanother aspect, R₂ is CH₂F, CHF₂, or CF₃.

In one aspect, R₃ is F. In a further aspect, R₃ is F and R₂ is H. Inanother aspect, R₃ is CH₂F, CHF₂, or CF₃. In a further aspect, R₃ isCF₃. In a further aspect, R₃ is CF₃ and R₂ is H.

In one aspect, R₂ and R₃ are each F.

In one aspect, Z is

and Q is

In a further aspect, Z is

Q is

and R and R′ are each H.

In a further aspect, Z is

Q is

R and R′ are each H; and R₁ is OCH₃, OCH₂F, OCHF₂, or OCF₃. In a furtheraspect, X is N and Y is CH; and R₁ is OCHF₂.

In one aspect, Z is

and Q is

In a further aspect, Z is

Q is

and X and Y are each N. In a further aspect, R₁ is methyl substitutedwith 1, 2, or 3 fluorine atoms. In a further aspect, R₁ is CF₃.

In another further aspect, Z is

Q is

and X is N and Y is CH. In a further aspect, R₁ is OCH₃, OCH₂F, OCHF₂,or OCF₃. In a further aspect, R₁ is OCHF₂.

In one aspect, Z is

and Q is

In one aspect, a compound of present invention is of formula II:

or a pharmaceutically acceptable salt or solvate thereof, wherein eachof the variables are as defined above. Compounds of the presentinvention include compounds of formula II, wherein the variables areillustrated in the various aspects of formula I above.

Representative compounds of the present invention include the compoundslisted in Table 1.

TABLE 1 Cmpd # Chemical Structure A1

A2

A3

A4

A5

A6

A7

A8

A9

 A10

 A11

 A12

 A13

 A14

In one aspect, a compound of the present invention is selected fromcompounds A1, A2, and A3, or a pharmaceutically acceptable salt orsolvate thereof. In a further aspect, a compound of the presentinvention is selected from compounds A1 and A2, or a pharmaceuticallyacceptable salt or solvate thereof. In a further aspect, a compound ofthe present invention is compound A1, or a pharmaceutically acceptablesalt or solvate thereof.

In one aspect, a compound of the present invention is a pharmaceuticallyacceptable salt. In one aspect, a compound of the present invention is asolvate. In a further aspect, a compound of the present invention is ahydrate.

In one aspect, a compound of the present invention inhibits the activityof αv integrins (e.g., αvβ3 and αvβ5) at a submicromolar concentration,e.g., below 1 μM, 0.8 μM, 0.6 μM, 0.5 μM, 0.2 μM, or 0.1 μM.

In one aspect, a compound of the present invention inhibits cellularadhesion to vitronectin through the αv integrin (e.g., αvβ3 and αvβ5) ator below an IC₅₀ of 2.0E-07 M using a human dermal microvascularendothelial cell (HMVEC) assay. In a further aspect, a compound of thepresent invention inhibits cellular adhesion to vitronectin through theαv integrin (e.g., αvβ3 and αvβ5) at or below an IC₅₀ of 2.5E-08 M usingan HMVEC assay. In a further aspect, a compound of the present inventioninhibits cellular adhesion to vitronectin through the αv integrin (e.g.,αvβ3 and αvβ5) at or below an IC₅₀ of 1.0E-08 M using an HMVEC assay. Inone aspect, a compound of the present invention inhibits cellularadhesion to vitronectin through the αv integrin (e.g., αvβ3 and αvβ5) ator below an IC₅₀ of 2.5E-07 M using a rat lung microvascular endothelialcell (RLMVEC) assay. In a further aspect, a compound of the presentinvention inhibits cellular adhesion to vitronectin through the αvintegrin (e.g., αvβ3 and αvβ5) at or below an IC₅₀ of 3.5E-08 M using anRLMVEC assay. In one aspect, a compound of the present inventioninhibits cellular adhesion to vitronectin through the αv integrin (e.g.,αvβ3 and αvβ5) at or below an IC₅₀ of 2.0E-08 M using a rabbit aorticendothelial cell (RAEC) assay. In a further aspect, a compound of thepresent invention inhibits cellular adhesion to vitronectin through theαv integrin (e.g., αvβ3 and αvβ5) at or below an IC₅₀ of 1.0E-08 M usingan RAEC assay.

In one aspect, a compound of the present invention inhibits or decreasesformation of blood vessels in a tissue or organ, in vivo or in vitro. Inone aspect, a compound of the present invention decreases the formationof blood vessels below 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10%, or5%, as compared to that in an untreated control. In a further aspect, acompound of the present invention decreases the formation of bloodvessels below 60%, 50%, 40%, 30%, 20%, 10%, or 5%, as compared to thatin an untreated control. In a further aspect, a compound of the presentinvention decreases the formation of blood vessels below 40%, 30%, 20%,10%, or 5%, as compared to that in an untreated control. In one aspect,the tissue is a tissue from the eye, such as a retinal tissue. In oneaspect, the organ is the eye.

In one aspect, a compound of the present invention is efficientlydistributed to the back of the eye, e.g., retina, after topicaladministration. In one aspect, a compound of the present invention isefficiently distributed to the retina within 12 hours, 10 hours, 8hours, 6 hours, 4 hours, 2 hours, or 1 hour, after topicaladministration to the eye. In a further aspect, a compound of thepresent invention is efficiently distributed to the retina within 8hours, 6 hours, 4 hours, 2 hours, or 1 hour, after topicaladministration to the eye.

Compounds of the present invention can be conveniently prepared by avariety of methods familiar to those skilled in the art. The compoundsof each of the formulae described herein may be prepared according tothe following procedures from commercially available starting materialsor starting materials which can be prepared using literature procedures.These procedures show the preparation of representative compounds ofthis invention. It is understood that compounds of the present inventionother than those illustrated in the following schemes can be made usingthese schemes with modifications commonly known in the art (e.g., usingdifferent starting material, changing reaction solvents, or adjustingreaction duration or temperature).

The compounds of the invention may contain one or more asymmetriccenters and can thus occur as racemates and racemic mixtures, singleenantiomers, diastereomeric mixtures and individual diastereomers.Additional asymmetric centers may be present depending upon the natureof the various substituents on the molecule. Each such asymmetric centerwill independently produce two optical isomers. It is intended that allof the possible optical isomers and diastereomers in mixtures and aspure or partially purified compounds are included within the ambit ofthe invention. The invention is meant to comprehend all such isomericforms of these compounds.

The independent syntheses of these diastereomers or theirchromatographic separations may be achieved as known in the art byappropriate modification of the methodology disclosed herein. Theirabsolute stereochemistry may be determined by the x-ray crystallographyof crystalline products or crystalline intermediates which arederivatized, if necessary, with a reagent containing an asymmetriccenter of known absolute configuration.

If desired, racemic mixtures of the compounds may be separated so thatthe individual enantiomers are isolated. The separation can be carriedout by methods well known in the art, such as contacting a racemicmixture of compounds with an enantiomerically pure compound to form adiastereomeric mixture, followed by separation of the individualdiastereomers by standard methods, such as fractional crystallization orchromatography. The diasteriomeric mixture is often a mixture ofdiasteriomeric salts formed by contacting a racemic mixture of compoundswith an enantiomerically pure acid or base. The diasteromericderivatives may then be converted to the pure enantiomers by cleavage ofthe added chiral residue. The racemic mixture of the compounds can alsobe separated directly by chromatographic methods utilizing chiralstationary phases, which are well known in the art.

Alternatively, any enantiomer of a compound may be obtained bystereoselective synthesis using optically pure starting materials orreagents of known configuration by methods well known in the art.

Some of the compounds of the invention may exist in unsolvated as wellas solvated forms such as, for example, hydrates.

“Solvate” means a solvent addition form that contains either astoichiometric or non-stoichiometric amounts of the solvent molecules.Some compounds have a tendency to trap a fixed molar ratio of thesolvent molecules in the crystalline solid state, thus forming asolvate. If the solvent is water, the solvate formed is a hydrate. Whenthe solvent is alcohol, the solvate formed is an alcoholate. Hydratesare formed by the combination of one or more molecules of water with oneof the substances (e.g., a compound of the invention) in which the waterretains its molecular state as H₂O, such combination being able to formone or more hydrate. In hydrates, the water molecules are attachedthrough secondary valencies by intermolecular forces, in particularhydrogen bridges. Solid hydrates contain water as so-called crystalwater in stoichiometric ratios, where the water molecules do not have tobe equivalent with respect to their binding state. Examples of hydratesinclude sesquihydrates, monohydrates, dehydrates, and trihydrates.Equally suitable are the hydrates of salts of the compounds of theinvention.

For use in medicine, the salts of the compounds of the invention referto non-toxic “pharmaceutically acceptable salts”. Other salts may,however, be useful in the preparation of the compounds of the inventionor pharmaceutically acceptable salts thereof. Salts encompassed withinthe term “pharmaceutically acceptable salts” refer to non-toxic salts ofthe compounds of the invention which can be prepared by reacting thefree base with a suitable organic or inorganic acid. Representativesalts include the following: acetate, benzenesulfonate, benzoate,bicarbonate, bisulfate, bitartrate, borate, bromide, camsylate,carbonate, chloride, clavulanate, citrate, dihydrochloride, edetate,edisylate, estolate, esylate, fumarate, gluceptate, gluconate,glutamate, glycollylarsanilate, hexylresorcinate, hydrabamine,hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isothionate,lactate, lactobionate, laurate, malate, maleate, mandelate, mesylate,methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate,N-methylglucamine ammonium salt, oleate, oxalate, pamottle (embonate),palmitate, pantothenate, phosphate/diphosphate, polygalacturonate,salicylate, stearate, sulfate, subacetate, succinate, tannate, tartrate,teoclate, tosylate, triethiodide, and valerate. Furthermore, where thecompounds of the invention carry an acidic moiety, suitablepharmaceutically acceptable salts thereof may include alkali metalsalts, e.g., sodium or potassium salts; alkaline earth metal salts,e.g., calcium or magnesium salts; and salts formed with suitable organicligands, e.g., quaternary ammonium salts which may be derived fromammonia or organic amines, such as, for example, diethylamine,triethylamine, ethyldiisopropylamine, procaine, dibenzylamine,N-methylmorpholine, dihydroabietylamine, or methylpiperidine.

The invention includes within its scope prodrugs of the compounds of theinvention. In general, such prodrugs will be functional derivatives ofthe compounds of the invention which are readily convertible in vivointo the required compound. Thus, in the methods of treatment of theinvention, the term “administering” shall encompass the treatment of thevarious disease and conditions described with the compound specificallydisclosed or with a compound which may not be specifically disclosed,but which converts to the specified compound in vivo afteradministration to the patient. Conventional procedures for the selectionand preparation of suitable prodrug derivatives are described, forexample, in “Design of Prodrugs,” ed. H. Bundgaard, Elsevier, 1985.Metabolites of these compounds include active species produced uponintroduction of compounds of the invention into the biological milieu.

The invention also includes one or more metabolites of a compound of theinvention.

The present invention also comprehends deuterium labeled compounds offormula I or II or the compounds listed in Table 1, wherein a hydrogenatom is replaced by a deuterium atom. The deuterium labeled compoundscomprise a deuterium atom having an abundance of deuterium that issubstantially greater than the natural abundance of deuterium, e.g.,0.015%.

The term “deuterium enrichment factor” as used herein means the ratiobetween the deuterium abundance and the natural abundance of adeuterium. In one aspect, a compound of the invention has a deuteriumenrichment factor for each deuterium atom of at least 3500 (52.5%deuterium incorporation at each deuterium atom), at least 4000 (60%deuterium incorporation), at least 4500 (67.5% deuterium incorporation),at least 5000 (75% deuterium), at least 5500 (82.5% deuteriumincorporation), at least 6000 (90% deuterium incorporation), at least6333.3 (95% deuterium incorporation), at least 6466.7 (97% deuteriumincorporation), at least 6600 (99% deuterium incorporation), or at least6633.3 (99.5% deuterium incorporation).

Deuterium labeled compounds can be prepared using any of a variety ofart-recognized techniques. For example, deuterium labeled compounds offormula I or II or the compounds listed in Table 1 can generally beprepared by carrying out the procedures disclosed in the Schemes and/orExamples described herein, by substituting a readily available deuteriumlabeled reagent for a non-deuterium labeled reagent.

A compound of the invention or a pharmaceutically acceptable salt orsolvate thereof that contains the aforementioned deuterium atom(s) iswithin the scope of the invention. Further, substitution with deuterium,i.e., ²H, can afford certain therapeutic advantages resulting fromgreater metabolic stability, for example, increased in vivo half-lifeand/or reduced dosage requirements.

In one aspect, the present invention relates to a method of synthesizinga compound of the invention or a pharmaceutically acceptable salt orsolvate thereof

Pharmaceutical Compositions of the Invention

The present invention relates to pharmaceutical compositions comprisinga compound of the invention as an active ingredient. In one aspect, theinvention provides a pharmaceutical composition comprising at least onecompound of formula I or II, or a pharmaceutically acceptable salt orsolvate thereof and one or more pharmaceutically acceptable carriers orexcipients. In one aspect, the invention provides a pharmaceuticalcomposition comprising at least one compound selected from Table 1. In afurther aspect, the invention provides a pharmaceutical compositioncomprising at least one compound selected from compounds A1, A2, and A3.In a further aspect, the invention provides a pharmaceutical compositioncomprising at least one compound selected from compounds A1 and A2. In afurther aspect, the invention provides a pharmaceutical compositioncomprising compound A1.

As used herein, the term “composition” is intended to encompass aproduct comprising the specified ingredients in the specified amounts,as well as any product which results, directly or indirectly, fromcombination of the specified ingredients in the specified amounts.

The compounds of the invention can be formulated for oral administrationin forms such as tablets, capsules (each of which includes sustainedrelease or timed release formulations), pills, powders, granules,elixirs, tinctures, suspensions, syrups and emulsions. The compounds ofthe invention can also be formulated for intravenous (bolus orin-fusion), intraperitoneal, topical (e.g., ocular eye-drop),subcutaneous, intramuscular or transdermal (e.g., patch) administration,all using forms well known to those of ordinary skill in thepharmaceutical arts. Preferably, compounds of the invention for thetreatment of macular degeneration, DR, DME, or macular edema followingRVO, are formulated for topical administration, for example, in the formof eye-drops.

For topical ocular administration, the compositions are provided asophthalmic formulation comprising a compound of the present invention inconcentration between about 0.01 and about 5 weight percent, preferablybetween about 0.1 and about 5.0 weight percent, more preferably betweenabout 0.5 and about 5.0 weight percent, and most preferably betweenabout 0.8 and about 3.0 weight percent.

The ophthalmic formulation of the present invention may be in the formof an aqueous solution comprising an aqueous vehicle.

The aqueous vehicle component of the ophthalmic formulation may comprisewater and at least one ophthalmically acceptable excipient. Preferably,the aqueous vehicle comprises a solution of the one or moreophthalmically acceptable excipients in water.

Suitable ophthalmically acceptable excipients include those selectedfrom the group consisting of a solubility enhancing agent, chelatingagent, preservative, tonicity agent, viscosity/suspending agent, buffer,and pH modifying agent, and a mixture thereof. Preferably, theophthalmically acceptable excipient is selected from the groupconsisting of a solubility enhancing agent, chelating agent,preservative, tonicity agent, viscosity/suspending agent, and pHmodifying agent, and a mixture thereof.

Any suitable ophthalmically acceptable solubility enhancing agent can beused. Examples of a solubility enhancing agent include cyclodextrin,such as those selected from the group consisting ofhydroxypropyl-β-cyclodextrin, methyl-β-cyclodextrin, randomlymethylated-β-cyclodextrin, ethylated-β-cyclodextrin,triacetyl-β-cyclodextrin, peracetylated-β-cyclodextrin,carboxymethyl-β-cyclodextrin, hydroxyethyl-β-cyclodextrin,2-hydroxy-3-(trimethylammonio)propyl-β-cyclodextrin,glucosyl-β-cyclodextrin, sulphated β-cyclodextrin (S-β-CD),maltosyl-β-cyclodextrin, β-cyclodextrin sulfobutyl ether,branched-β-cyclodextrin, hydroxypropyl-γ-cyclodextrin, randomlymethylated-γ-cyclodextrin, and trimethyl-γ-cyclodextrin, and mixturesthereof. Preferably, solubility enhancing agent includes β-cyclodextrinsulfobutyl ether, hyrdoxypropyl-β-cyclodextrin, sulphated β-cyclodextrin(S-β-CD), and maltosyl-β-cyclodextrin, and mixtures thereof.β-cyclodextrin sulfobutyl ether is a particularly preferred solubilityenhancing agent. The solubility enhancing agent(s) may be added in anamount of about 1 to about 20 wt %, preferably about 1 to about 10 wt %,and more preferably about 5 to about 10 wt %.

Any suitable ophthalmically acceptable chelating agent can be used.Examples of a suitable ophthalmically acceptable chelating agent includethose selected from the group consisting of ethylenediaminetetraaceticacid and metal salts thereof, disodium edetate, trisodium edetate, andtetrasodium edetate, and mixtures thereof. Disodium edetate is aparticularly preferred chelating agent. The chelating agent(s) may beadded in an amount of about 0.001 to about 0.05 wt %, preferably about0.001 to about 0.02 wt %, more preferably about 0.002 to about 0.01 wt%, and most preferably about 0.002 to about 0.005 wt %.

Preferably, the aqueous vehicle includes a preservative. Preferredpreservatives include those selected from the group consisting ofquaternary ammonium salts such as benzalkonium halides (preferablybenzalkonium chloride), chlorhexidine gluconate, benzethonium chloride,cetyl pyridinium chloride, benzyl bromide, phenylmercury nitrate,phenylmercury acetate, phenylmercury neodecanoate, merthiolate,methylparaben, propylparaben, sorbic acid, potassium sorbate, sodiumbenzoate, sodium propionate, ethyl p-hydroxybenzoate, propylaminopropylbiguanide, and butyl-p-hydroxybenzoate, sorbic acid, and mixturesthereof. More preferably, the preservative is a quaternary ammonium saltsuch as benzalkonium halides (preferably benzalkoniurn chloride),chlorhexidine gluconate, benzethonium chloride, cetyl pyridiniumchloride, potassium sorbate, sodium benzoate, ethyl p-hydroxybenzoate,butyl p-hydroxybenzoate, or propylaminopropyl biguanide, or mixturesthereof. Propylaminopropyl biguanide is an especially preferredpreservative. The preservative(s) may be used in an amount of about0.00001 to about 0.0001 wt %, preferably about 0.00001 to about 0.00008wt %, and more preferably about 0.00002 to about 0.00005 wt %.

The aqueous vehicle may also include a tonicity agent to adjust thetonicity (osmotic pressure) in order to achieve an ophthalmicallycompatible formulation. The tonicity agent can be selected from thegroup consisting of a glycol (such as propylene glycol, diethyleneglycol, triethylene glycol), glycerol, dextrose, glycerin, mannitol,potassium chloride, and sodium chloride, and a mixture thereof.Preferably, the tonicity agent is selected from the group consisting ofglycerin, mannitol, potassium chloride, and sodium chloride. Morepreferably mannitol and/or sodium chloride (and most preferably amixture thereof) are employed. The tonicity agent(s) may be used in anamount of about 0.05 to about 8 wt %, preferably about 0.1 to about 6 wt%, more preferably about 0.1 to about 4 wt %, and most preferably about0.2 to about 4 wt %.

When a mixture of mannitol and sodium chloride is used as tonicityagents, preferably the weight ratio of mannitol:sodium chloride is about4:1 to about 15:1, more preferably about 6:1 to about 14:1, or 8:1 toabout 14:1 and particularly about 10:1 to about 12:1. If mannitol aloneis used as the tonicity agent, it is preferably used in an concentrationof about 4.5 to about 6.5 wt %, and more preferably in a concentrationof about 5.0 to about 5.5 wt %. If sodium chloride alone is used as thetonicity agent, it is used in a concentration of about 0.05 to about 8wt %, preferably about 0.1 to about 6 wt %, more preferably about 0.1 toabout 4 wt %, and most preferably about 0.2 to about 4 wt %.

The aqueous vehicle preferably also contains a viscosity/suspendingagent. Suitable viscosity/suspending agents include those selected fromthe group consisting of cellulose derivatives, such as methyl cellulose,ethyl cellulose, hydroxyethylcellulose, polyethylene glycols (such aspolyethylene glycol 300, polyethylene glycol 400), carboxymethylcellulose, hydroxypropylmethyl cellulose, and cross-linked acrylic acidpolymers (carbomers), such as polymers of acrylic acid cross-linked withpolyalkenyl ethers or divinyl glycol (Carbopols—such as Carbopol 934,Carbopol 934P, Carbopol 971, Carbopol 974 and Carbopol 974P), and amixture thereof. In preferred embodiments of the present invention, theviscosity/suspending agent is a carbomer, more preferably Carbopol 974P.The viscosity/suspending agent(s) may be present in an amount of about0.05 to about 2 wt %, preferably 0.1 to about 1 wt %, more preferablyabout 0.2 to about 0.8 wt %, and most preferably about 0.3 to about 0.5wt %.

In order to adjust the formulation to an ophthalmically acceptable pH(typically a pH range of about 5.0 to about 9.0, more preferably about5.5 to about 8.5, particularly about 6.0 to about 8.5, about 7.0 toabout 8.5, about 7.2 to about 7.7, about 7.1 to about 7.9, or about 7.5to about 8.0), the formulation may contain a pH modifying agent. The pHmodifying agent is typically a mineral acid or metal hydroxide base,selected from the group of potassium hydroxide, sodium hydroxide, andhydrochloric acid, and mixtures thereof, and preferably sodium hydroxideand/or hydrochloric acid. These acidic and/or basic pH modifying agentsare added to adjust the formulation to the target ophthalmicallyacceptable pH range. Hence it may not be necessary to use both acid andbase—depending on the formulation, the addition of one of the acid orbase may be sufficient to bring the mixture to the desired pH range.

The aqueous vehicle may also contain a buffering agent to stabilize thepH. When used, the buffer is selected from the group consisting of aphosphate buffer (such as sodium dihydrogen phosphate and disodiumhydrogen phosphate), a borate buffer (such as boric acid, or saltsthereof including disodium tetraborate), a citrate buffer (such ascitric acid, or salts thereof including sodium citrate), andε-aminocaproic acid, and mixtures thereof. The buffer agent(s) may bepresent in an amount of about 0.05 to about 5 wt %, preferably 0.1 toabout 5 wt %, more preferably about 0.2 to about 5 wt %, and mostpreferably about 0.5 to about 5 wt %.

The ophthalmic formulation for topical administration to the eye mayfurther comprise a wetting agent. In any embodiment of the presentinvention the wetting agent is preferably a non-ionic wetting agent.More preferably, the wetting agent is water soluble or swellable. Mostpreferably the wetting agent is water soluble. “Water soluble” is to beunderstood in the manner used in standard texts such as the “Handbook ofPharmaceutical Excipients” (Raymond C Rowe, Paul J Sheskey and Sian COwen, Fifth Edition, Pharmaceutical Press and American PharmacistsAssociation 2006). Suitable classes of wetting agents include thoseselected from the group consisting of polyoxypropylene-polyoxyethyleneblock copolymers (poloxamers), polyethoxylated ethers of castor oils,polyoxyethylenated sorbitan esters (polysorbates), polymers ofoxyethylated octyl phenol (Tyloxapol), polyoxyl 40 stearate, fatty acidglycol esters, fatty acid glyceryl esters, sucrose fatty esters, andpolyoxyethylene fatty esters, and mixtures thereof.

Specific examples of suitable wetting agents include those selected fromthe group consisting of: polyoxyethylene-polyoxypropylene blockcopolymers (poloxamers) such as: polyoxyethylene (160) polyoxypropylene(30) glycol [Pluronic F68], polyoxyethylene (42) polyoxypropylene (67)glycol [Pluronic P123], polyoxyethylene (54) polyoxypropylene (39)glycol [Pluronic P85], polyoxyethylene (196) polyoxypropylene (67)glycol [Poloxamer 407, Pluronic F127], polyoxyethylene (20)polyoxypropylene (20) glycol [Pluronic L44], polyoxyethylenated sorbitanesters (polysorbates) such as poly(oxyethylene)sorbitan monopalmitate(polysorbate 40), poly(oxyethylene)sorbitan monostearate (polysorbate60), poly(oxyethylene)sorbitan tristearate (polysorbate 65),poly(oxyethylene) sorbitan monooleate (polysorbate 80),poly(oxyethylene) sorbitan monolaurate, poly(oxyethylene) sorbitantrioleate, polyethoxylated ethers of castor oils such as polyoxyethylenehydrogenated castor oil 10, polyoxyethylene hydrogenated castor oil 40,polyoxyethylene hydrogenated castor oil 50 and polyoxyethylenehydrogenated castor oil 60, polyoxyl 40 stearate, sucrose fatty esters,and polyoxyethylene fatty esters, and mixtures thereof.

Preferably, the wetting agent is selected from the group consisting of:polyoxyethylene-polyoxypropylene block copolymers (poloxamers) such as:polyoxyethylene (160) polyoxypropylene (30) glycol [Pluronic F68],polyoxyethylene (42) polyoxypropylene (67) glycol [Pluronic P123],polyoxyethylene (54) polyoxypropylene (39) glycol [Pluronic P85],polyoxyethylene (196) polyoxypropylene (67) glycol [Poloxamer 407,Pluronic F127], and polyoxyethylene (20) polyoxypropylene (20) glycol[Pluronic L44], polyoxyethylenated sorbitan esters (polysorbates) suchas poly(oxyethylene)sorbitan monopalmitate (polysorbate 40),poly(oxyethylene)sorbitan monosteaxate (polysorbate 60),poly(oxyethylene)sorbitan tristearate (polysorbate 65),poly(oxyethylene) sorbitan monooleate (polysorbate 80),poly(oxyethylene) sorbitan monolaurate, and poly(oxyethylene) sorbitantrioleate and mixtures thereof.

More preferably, the wetting agent is a polyoxyethylene-polyoxypropyleneblock copolymer (poloxamer). Examples of suitable poloxamers include:polyoxyethylene (160) polyoxypropylene (30) glycol [Pluronic F68],polyoxyethylene (42) polyoxypropylene (67) glycol [Pluronic P123],polyoxyethylene (54) polyoxypropylene (39) glycol [Pluronic P85],polyoxyethylene (196) polyoxypropylene (67) glycol [Poloxamer 407,Pluronic F127] and polyoxyethylene (20) polyoxypropylene (20) glycol[Pluronic L44] or a mixture thereof.

Further preferred are wetting agents selected from the group consistingof polyoxyethylene (42) polyoxypropylene (67) glycol [Pluronic PI 23],polyoxyethylene (54) polyoxypropylene (39) glycol [Pluronic P85],polyoxyethylene (196) polyoxypropylene (67) glycol [Poloxamer 407,Pluronic F127] and mixtures thereof.

An especially preferred wetting agent is polyoxyethylene (196)polyoxypropylene (67) glycol [Poloxamer 407, Pluronic F127].

Particularly preferred formulations for topical administration to theeye of the present invention comprise a compound of the presentinvention, a solubility enhancing agent, a cheating agent, apreservative, a tonicity agent, a viscosity/suspending agent, a buffer,and a pH modifying agent. More particularly preferred formulations arecomprised of an aqueous solution of a β-cyclodextrin, a borate salt,boric acid, sodium chloride, disodium edetate, and propylaminopropylbiguanide.

In one aspect, the ophthalmic formulation of the present invention is inthe form of a solution, such as one of the following:

Solution Composition a compound of the invention 0.1-5.0 g a solubilityenhancing agent 1-20 g a buffering agent 0.05-5.0 g an tonicity agent0.05-8 g a chelating agent 1-50 mg a preservative 0.01-0.1 mg water 100ml

Solution Composition a compound of the invention 0.8-3.0 g a solubilityenhancing agent 5-10 g a buffering agent 0.5-5.0 g an tonicity agent0.2-4 g a chelating agent 2-5 mg a preservative 0.02-0.05 mg water 100ml

Solution Composition I II III IV a compound of the 2.5 g 2.0 g 1.5 g 1.0g invention a solubility enhancing 10 g 10 g 10 g 5 g agent bufferingagent 1 1.05 g 1.05 g 1.05 g 1.05 g buffering agent 2 0.285 g 0.285 g0.285 g 0.285 g an tonicity agent 0.25 g 0.25 g 0.25 g 0.25 g achelating agent 2.5 mg 2.5 mg 2.5 mg 2.5 mg a preservative 0.03 mg 0.03mg 0.03 mg 0.03 mg water 100 ml 100 ml 100 ml 100 ml

The ophthalmic formulation of the present invention may also be in theform of a gel or a semi-gel, or both; a jelly; a suspension; anemulsion; an oil; an ointment; a cream; or a spray.

The ophthalmic gel, semi-gel, jelly, suspension, emulsion, oil,ointment, cream, or spray may contain various additives incorporatedordinarily, such as buffering agents (e.g., phosphate buffers, boratebuffers, citrate buffers, tartrate buffers, acetate buffers, aminoacids, sodium acetate, sodium citrate and the like), tonicity agents(e.g., saccharides such as sorbitol, glucose and mannitol, polyhydricalcohols such as glycerin, concentrated glycerin, PEG and propyleneglycol, salts such as sodium chloride), preservatives or antiseptics(e.g., benzalkonium chloride, benzalkonium chloride, P-oxybenzoates suchas methyl p-oxybenzoate or ethyl p-oxybenzoate, benzyl alcohol,phenethyl alcohol, sorbic acid or its salt, thimerosal, chlorobutanoland the like), solubilizing enhancing agents (e.g., cyclodextrins andtheir derivative, water-soluble polymers such as polyvinyl pyrrolidone,surfactants such as tyloxapol, polysorbates), pH modifiers (e.g.,hydrochloric acid, acetic acid, phosphoric acid, sodium hydroxide,potassium hydroxide, ammonium hydroxide and the like), thickening agents(e.g., HEC, hydroxypropyl cellulose, methyl cellulose, HPMC,carboxymethyl cellulose and their salts), chelating agents (e.g., sodiumedetate, Sodium citrate, condensed sodium phosphate) and the like. Eachof these additives may be in the amount or concentration similar tothose described for the ophthalmic formulation in the form of a solutionabove.

Furthermore the compounds of the invention may be formulated for topicaladministration by incorporation into novel ophthamlic formulationsincluding but not limited to: microemulsions, liposomes, niosomes, gels,hydrogel, nanoparticles, and nanosuspension.

1. Microemulsions

Microemulsions are dispersion of water and oil facilitated by acombination of surfactant and cosurfactant in a manner to reduceinterfacial tension. These systems are usually characterized by higherthermodynamic stability, small droplet size (approximately 100 nm) andclear appearance. Their transparent appearance is due to the high levelof dispersion of the internal phase, and the size of it ranges from100-1000 angstroms. Processes for forming microemulsions suitable foruse in ophthalmic formulations are described in Vandamme TF. ProgRetinal Eye Res 2002; 21:15-34, which is incorporated by reference.

2. Liposomes

Liposomes are lipid vesicles containing aqueous core and have beenwidely exploited in ocular delivery for various drug substances.Depending on the nature of the lipid composition selected, liposomes canprovide extended release of the drug.

3. Niosomes

Niosomes are bilayered structural vesicles made up of nonionicsurfactant and are capable of encapsulating both lipophilic andhydrophilic compounds. They can release the drug independent of pH andenhance ocular bioavailability. Niosomes are microscopic lamellarstructures that are formed on the admixture of nonionic surfactant ofthe alkyl or diakyl polyglycerol ether class and cholesterol withsubsequent hydration in aqueous media. Structurally niosomes are similarto liposomes, in that they are also made up of a bilayer. However, thebilayer in the case of nisomes is made up of nonionic surface-activeagents rather than phospholipids as in the case of liposomes. Niosomesmay be unilamellar or multilamellar depending on the method used toprepare them. They are capable of entrapping hydrophilic and hydrophobicsolutes. They possess great stability and lack many disadvantagesassociate with liposomes such as high cost and the variable purity ofphospholipids. The properties of niosomes and process for preparing themare well known in the art, see e.g., Wagh V D et al., J Pharm Res 2010;3(7):1558-1563; Kaur H et al., Int J Pharm Sci Rev Res 2012;15(1):113-120, each of which is incorporated by reference.

4. Gels

Ophthalmic gels are composed of mucoadhesive polymers that providelocalized delivery of an active ingredient to the eye. Such polymershave a property known as bioadhesion, meaning attachment of a drugcarrier to a specific biological tissue. These polymers are able toextend the contact time of the drug with the biological tissues andthereby improve ocular bioavailability. The choice of the polymer playsa critical role in the release kinetics of the drug from the dosageform. Several bioadhesive polymers are available with varying degree ofmucoadhesive performance. Some examples are carboxymethylcellulose,carbopol, polycarbophil, and sodium alginate. The use of gelformulations in ocular drug deliver has been reviewed in Ali Y et al.,Adv Drug Deliv Rev 2006; 58: 1258-1268, which is incorporated byreference.

5. Hydrogels

Hydrogels are three-dimensional, hydrophilic, polymeric networks capableof taking in large amounts of water or biological fluids. Residence timecan be significantly enhanced with a hydrogel formulation. The gelationcan be obtained by changing temperature and pH. Poloxamers, the mostwidely used polymer, contains the hydrophobic part in the centresurrounded by a hydrophilic part. Though they are widely employed toenhance the residence time. Recent perspectives in the use of hydrogelsin ocular drug deliver are described by Gaudana R, Jwala J, Boddu S H S,Mitra A K. Pharm Res. 2009; 26(5):1197-1216 which is incorporated byreference.

6. Nanoparticles

Nanoparticles are defined as particles with a diameter of less than 1μm, comprising of various biodegradable or non biodegradable polymers,lipids, phospholipids or metals. They can be classified as nanospheresor nanocapsules depending upon whether the drug has been uniformlydispersed or coated within polymeric material. The uptake anddistribution of nanoparticles is dependent on their size. The use ofnanoparticles in ocular drug delivery has recently been reviewed by Hinget al., Int. J. Ophthalmol 2013; 6:390-396, which is incorporated byreference.

7. Nanosuspensions

Nanosuspensions are defined as sub-micron colloidal systems that consistof poorly water soluble drugs suspended in an appropriate dispersionmedium stabilized by surfactants. Usually, nanosuspensions consist ofcolloidal carriers like polymeric resins which are inert in nature.Nanosuspensions enhance drug solubility and thus bioavailability. Unlikemicroemulsions, nanosuspensions are non-irritant. Charge on the surfaceof nanoparticles facilitates their adhesion to the cornea. The use ofnanosuspensions in drug delivery is reviewed in Rabinow, Nature Rev DrugDisc 2004; 785-796, which is incorporated by reference.

The compounds of the present invention can also be administered in theform of a formulation suitable for ocular topical delivery. Detaileddescriptions of formulation suitable for ocular topical delivery aredescribed in J. D. Bartlett and S. D. Jaanus, “Clinical OcularPharmacology”, 2008, Elsevier Health Sciences, which is incorporated byreference.

The compounds of the invention may also be coupled with soluble polymersas targetable drug carriers. Such polymers can includepolyvinylpyrrolidone, pyran copolymer,polyhydroxypropylmethacrylamide-phenol,polyhydroxyethylaspartamide-phenol, and polyethyleneoxide-polylysinesubstituted with palmitoyl residues. Furthermore, the compounds of theinvention may be coupled to a class of biodegradable polymers useful inachieving controlled release of a drug, for example, polylactic acid,polyglycolic acid, copolymers of polylactic and polyglycolic acid,polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters,polyacetals, polydihydropyrans, polycyanoacrylates and crosslinked oramphipathic block copolymers of hydrogels.

The present invention also provides a pharmaceutical compositioncomprising a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof, and a pharmaceutically acceptable carrier orexcipient, and further an active ingredient selected from the groupconsisting of a) an antagonist of integrin α5β1, b) acytotoxic/antiproliferative agent, c) an inhibitor of epidermal-derived,fibroblast-derived, or platelet-derived growth factor, d) an inhibitorof VEGF, e) an inhibitor of Flk-1/KDR, Flt-1, Tck/Tie-2, or Tic-1, andf) an inhibitor of phosphoinositide 3-kinase, and a mixture thereof.

The present invention further provides a pharmaceutical compositioncomprising a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof, and a pharmaceutically acceptable carrier orexcipient, and further an active ingredient selected from the groupconsisting of a) an antagonist of integrin α5β1, b) acytotoxic/antiproliferative agent, c) an inhibitor of epidermal-derived,fibroblast-derived, or platelet-derived growth factors, d) an inhibitorof VEGF, and e) an inhibitor of phosphoinositide 3-kinase, and a mixturethereof.

Nonlimiting examples of antagonists of integrin α5β1 are(S)-2-((R)-2-((S)-2-((S)-2-((S)-1-acetylpyrrolidine-2-carboxamido)-3-(1H-imidazol-5-yl)propanamido)-3-hydroxypropanamido)-3-mercaptopropanamido)succinamide,and JSM6427, described in Stragies, R. et al., J. Med. Chem. 2007,50:3786-3794, herein incorporated by reference.

Nonlimiting examples of cytotoxic/antiproliferative agents are taxol,vincristine, vinblastine, and doxorubicin.

Nonlimiting examples of inhibitors of epidermal-derived,fibroblast-derived, or platelet-derived growth factors are pazopanib,and sunitinib,

Nonlimiting examples of inhibitors of vascular endothelial derivedgrowth factor (VEGF) are bevacizumab and ranibizumab,

Nonlimiting examples of inhibitors of phosphoinositide 3-kinase areindelalisib and 2-morpholin-4-yl-8-phenylchroman-4-one.

Methods of Use

Compounds of the invention typically display submicromolar inhibitoryactivity for the integrins αv, such as αvβ3 and αvβ5. Inhibiting thefunction of αvβ3 and αvβ5 integrins prevents endothelial cellproliferation. Endothelial cell proliferation can result in deleteriousneovascularization or angiogenesis, particularly choroidalneovascularization in the choriocapillaris, through Bruch's membrane,ultimately leading to blood and protein leakage below the macula.Bleeding, leaking, and scarring from these blood vessels eventuallycause irreversible damage to the photoreceptors and rapid vision loss ifleft untreated.

Diabetic retinopathy, a closely related condition, is the result ofmicrovascular retinal changes. Hyperglycemia-induced intramural pericytedeath and thickening of the basement membrane lead to incompetence ofthe vascular walls in the retina, which affects the blood-retinalbarrier and makes the retinal blood vessels more permeable. Damagedblood vessels leak fluid and lipids onto the macula, the part of theretina that provides us with detailed vision, causing the macula toswell. Eventually this can progress to develop a condition calledmacular edema.

Accordingly, AMD, DR, DME, and macular edema following central retinalvein occlusion (thrombosis) can be treated or prevented throughadministration (e.g., topical administration) of the compounds orpharmaceutical compositions of the present invention.

The present invention provides a method of treating or preventing adisease or condition in a subject, comprising administering to a subjectin need thereof a therapeutically effective amount of a compound of theinvention or a pharmaceutically acceptable salt or solvate thereof or atherapeutically effective amount of a pharmaceutical composition of theinvention. In one aspect, the invention provides treating a disease orcondition. In one aspect, the invention provides preventing a disease orcondition.

In one aspect, the compound or pharmaceutical composition of theinvention is administered topically. In a further aspect, the compoundor pharmaceutical composition of the invention is administered as anophthalmic solution. In another aspect, the compound or pharmaceuticalcomposition of the invention is administered as an ophthalmic emulsion,suspension, gel, or semi-gel. In another aspect, the compound orpharmaceutical composition of the invention is administered as anophthalmic jelly, oil, ointment, cream, or spray.

The compounds or pharmaceutical compositions of the invention areadministered in dosages effective to inhibit the function of αvβ3 and/orαvβ5 integrins and thus treat or prevent a disease condition mediated bythe αvβ3 and/or αvβ5 integrin.

The present invention provides a method of treating or preventing adisease or condition mediated by an αv integrin in a subject, comprisingadministering to a subject in need thereof a therapeutically effectiveamount of a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof or a therapeutically effective amount of apharmaceutical composition of the invention. In one aspect, the diseaseor condition is a disease or condition in which angiogenesis isinvolved. In a further aspect, the disease or condition is a disease orcondition in which ocular angiogenesis is involved.

The present invention also provides a method of treating or preventingan αvβ3 and/or αvβ5 integrin-mediated disease or condition in a subject,comprising administering to a subject in need thereof a therapeuticallyeffective amount of a compound of the invention or a pharmaceuticallyacceptable salt or solvate thereof or a therapeutically effective amountof a pharmaceutical composition of the invention. In one aspect, thedisease or condition is a disease or condition in which ocularangiogenesis is involved. In one aspect, the disease or condition ismacular degeneration. In one aspect, the disease or condition isage-related macular degeneration (AMD). In one aspect, the disease orcondition is diabetic retinopathy (DR). In one aspect, the disease orcondition is diabetic macular edema (DME). In one aspect, the disease orcondition is macular edema following retinal vein occlusion (RVO).

The present invention further provides a method of treating orpreventing AMD, DR, DME, or macular edema following RVO, comprisingadministering to a subject in need thereof, a therapeutically effectiveamount of a compound of the invention or a pharmaceutically acceptablesalt or solvate thereof or a therapeutically effective amount of apharmaceutical composition of the invention. In one aspect, theinvention provides treating AMD, DR, DME, or macular edema followingRVO. In one aspect, the invention provides preventing AMD, DR, DME, ormacular edema following RVO.

The present invention further provides a method of treating orpreventing a disease or condition in a subject, comprising administeringto a subject in need thereof a therapeutically effective amount of acompound of the invention or a pharmaceutically acceptable salt orsolvate thereof or a therapeutically effective amount of apharmaceutical composition of the invention, in combination with asecond therapy for treating or preventing the disease or condition. Inone aspect, the disease or condition is mediated by an αv integrin. In afurther aspect, the disease or condition is mediated by an αvβ3 and/orαvβ5 integrin. In one aspect, the disease or condition is a disease orcondition in which angiogenesis is involved. In a further aspect, thedisease or condition is a disease or condition in which ocularangiogenesis is involved. In one aspect, the second therapy comprisesadministration of one or more of the following: a) an antagonist ofintegrin α5β1, b) a cytotoxic/antiproliferative agent, c) an inhibitorof epidermal-derived, fibroblast-derived, or platelet-derived growthfactor, d) an inhibitor of VEGF, e) an inhibitor of Flk-1/KDR, Flt-1,Tck/Tie-2, or Tic-1, and f) an inhibitor of phosphoinositide 3-kinase,and a mixture thereof. In a further aspect, the second therapy comprisesadministration of one or more of the following: a) an antagonist ofintegrin α5β1, b) a cytotoxic/antiproliferative agent, c) an inhibitorof epidermal-derived, fibroblast-derived, or platelet-derived growthfactor, d) an inhibitor of VEGF, and e) an inhibitor of phosphoinositide3-kinase, and a mixture thereof. In a further aspect, the second therapycomprises administration of an inhibitor of VEGF. In a further aspect,the VEGF inhibitor is bevacizumab or ranibizumab.

The second therapy can be administered via any administration routes,including oral administration in forms such as tablets, capsules (eachof which includes sustained release or timed release formulations),pills, powders, granules, elixirs, tinctures, suspensions, syrupsemulsions, intravenous administration (bolus or in-fusion),intraperitoneal administration, topical administration (e.g., oculareye-drop), subcutaneous administration, intramuscular administration,transdermal (e.g., patch) administration, and intravitrealadministration. In one aspect, the second therapy is administeredthrough intravitreal injection.

Administration of the second therapy in combination typically is carriedout over a defined time period (usually minutes, hours, days or weeksdepending upon the combination selected). “Combination therapy” may be,but generally is not, intended to encompass the administration of two ormore of these therapeutic agents as part of separate monotherapyregimens that incidentally and arbitrarily result in the combinations ofthe present invention. “Combination therapy” is intended to embraceadministration of these therapeutic agents in a sequential manner,wherein each therapeutic agent is administered at a different time, aswell as administration of these therapeutic agents, or at least two ofthe therapeutic agents, in a substantially simultaneous manner.

In accordance with the method of the invention, the individualcomponents of the combination can be administered separately atdifferent times during the course of therapy or concurrently in dividedor single combination forms. The instant invention is therefore to beunderstood as embracing all such regimens of simultaneous or alternatingtreatment, and the term “administering” is to be interpretedaccordingly. It will be understood that the scope of combinations of thecompounds of the invention with other agents useful for treating αvintegrin-mediated conditions includes in principle any combination withany pharmaceutical composition useful for treating macular degeneration,DR, DME, or macular edema following RVO. When the method of theinvention is a combination treatment of a formulation of the presentinvention topically administered to the eyes and an anti-VEGF protein oraptamer, the procedures, dosages and frequencies of the anti-VEGFprotein or aptamer are as described in the package inserts for thoseagents.

The dosage regimen utilizing the compounds of the invention is selectedin accordance with a variety of factors including type, species, age,weight, sex and medical condition of the patient; the severity of thecondition to be treated; and the particular compound or salt thereofemployed. An ordinary skilled physician, veterinarian or clinician canreadily determine and prescribe the effective amount of the drugrequired to prevent, counter or arrest the progress of the condition.

In the methods of the invention, the compounds herein described indetail can form the active ingredient, and are typically administered inadmixture with suitable pharmaceutical diluents, excipients or carriers(collectively referred to herein as “carrier”) suitably selected withrespect to the intended topical administration to the eye and consistentwith conventional pharmaceutical practices.

For purposes of the invention, the following definitions will be used(unless expressly stated otherwise):

“A compound of the invention”, “compounds of the invention”, “a compoundof the present invention”, or “compounds of the present invention”refers to a compound(s) disclosed herein, e.g., a compound(s) of theinvention includes a compound(s) of any of the formulae described hereinincluding formula I and II and/or a compound(s) explicitly disclosedherein. Whenever the term is used in the context of the invention it isto be understood that the reference is being made to the free base andthe corresponding pharmaceutically acceptable salts or solvates thereof,provided that such is possible and/or appropriate under thecircumstances.

“Pharmaceutical” or “pharmaceutically acceptable” when used herein as anadjective, means substantially non-toxic and substantiallynon-deleterious to the recipient.

By “pharmaceutical composition” it is further meant that the carrier,diluent, solvent, excipient, and salt must be compatible with the activeingredient of the formulation (e.g., a compound of the invention). It isunderstood by those of ordinary skill in this art that the terms“pharmaceutical formulation” and “pharmaceutical composition” aregenerally interchangeable, and they are so used for the purposes of thisapplication.

“Solution” refers to a clear, homogeneous liquid dosage form thatcontains one or more chemical substances dissolved in a solvent ormixture of mutually miscible solvents. Because molecules of atherapeutic agent substance in solution are uniformly dispersed, the useof solutions as dosage forms generally provides assurance of uniformdosage upon administration and good accuracy when the solution isdiluted or otherwise mixed. “Solution” as disclosed herein contemplatesany variations based on the current state of the art or variationsachieved by one skilled in the art.

“Suspension” refers to a liquid dosage form that contains solidparticles dispersed in a liquid vehicle. “Suspension” as disclosedherein contemplates any variations based on the current state of the artor variations achieved by one skilled in the art.

“Excipient” is used herein to include any other compound that is not atherapeutically or biologically active compound and may be contained inor combined with one or more of the compounds of the present invention.As such, an excipient should be pharmaceutically or biologicallyacceptable or relevant (for example, an excipient should generally benon-toxic to the subject). “Excipient” includes a single such compoundand is also intended to include a plurality of excipients. For thepurposes of the present disclosure the term “excipient” and “carrier”are used interchangeably throughout the description of the presentapplication.

“Therapeutically effective amount” refers to that amount of a drug orpharmaceutical agent that will elicit the biological or medical responseof a tissue, system, animal, or human that is being sought by aresearcher or clinician.

“Treat,” “treating,” or “treatment” refers to decreasing the symptoms,markers, and/or any negative effects of a disease or condition in anyappreciable degree in a subject who currently has the disease orcondition. In some embodiments, treatment may be administered to asubject who exhibits only early signs of a disease or condition for thepurpose of decreasing the risk of developing the disease or condition.In some embodiments, “Treat,” “treating,” or “treatment” refers toamelioration of one or more symptoms of a disease or condition. Forexample, amelioration of one or more symptoms of a disease or conditionincludes a decrease in the severity, frequency, and/or length of one ormore symptoms of a disease or condition.

“Prevent,” “prevention,” or “preventing” refers to any method topartially or completely prevent or delay the onset of one or moresymptoms or features of a disease or condition. Prevention may beadministered to a subject who does not exhibit any sign of a disease orcondition.

“Subject” means a human or animal (in the case of an animal, moretypically a mammal). In one aspect, the subject is a human.

The term “symptom” is defined as an indication of disease, illness,injury, or that something is not right in the body. Symptoms are felt ornoticed by the individual experiencing the symptom, but may not easilybe noticed by others. Others are defined as non-health-careprofessionals.

“αv integrin antagonist” refers to a compound which binds to andinhibits or interferes with the function of either αvβ3 or αvβ5, or acompound which binds to and inhibits or interferes with the function ofboth αvβ3 and αvβ5 (i.e., a dual αvβ3/αvβ5 antagonist). The compoundsbind to the receptors as antagonists, blocking or interfering with thebinding of the native agonist, such as vitronectin, while not provokinga biological response themselves.

“Bone resorption” refers to the process by which osteoclasts degradebone.

“Alkyl” refers to straight chain or branched alkyl of the number ofcarbon atoms specified (e.g., C₁-C₄ alkyl), or any number within thisrange (methyl, ethyl, propyl, i-propyl, butyl, i-butyl, t-butyl, etc.).

“Alkoxy” refers to straight chain or branched alkoxides of the number ofcarbon atoms specified (e.g., C₁-C₆ alkoxy), or any number within thisrange (methoxy, ethoxy, propoxy, i-propoxy, butoxy, i-butoxy, t-butoxy,etc.).

“Carbocyclic ring” refers to saturated cycloalkyl of the number ofcarbon atoms specified (i.e., C₃ or C₄), such as cyclopropyl andcyclobutyl.

“Heterocyclic ring” refers to saturated heterocyclic ring of the numberof carbon atoms specified (i.e., C₃ or C₄), further comprising oneadditional heteroatoms selected from N, O, and S.

The term “about” refers to a range of values which can be 15%, 10%, 8%,5%, 3%, 2%, 1%, or 0.5% more or less than the specified value. Forexample, “about 10%” can be from 8.5% to 11.5%. In one embodiment, theterm “about” refers to a range of values which are 5% more or less thanthe specified value. In another embodiment, the term “about” refers to arange of values which are 2% more or less than the specified value. Inanother embodiment, the term “about” refers to a range of values whichare 1% more or less than the specified value.

EXAMPLES Example 1 Synthesis of(S)-3-(6-(difluoromethoxy)-pyridine-3-yl)-3-(2-oxo-3-(3-(5, 6, 7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl)imidazolidin-1-yl) propanoicacid (Compound A1)

Compound A1 is made using a convergent synthesis scheme as shown inScheme 1: fragment 6b is reacted with fragment 9 to form compound 10,which is further reacted in three steps to form Compound A1.

Synthesis of Fragment 6b

tert-butyl 2-oxopyrrolidine-1-carboxylate (2a): To a stirred solution ofcompound 1a (10.0 g, 117 mmol, 1.0 equiv.) in DCM, (Boc)₂O (25.5 g, 117mmol, 1.00 equiv.) and DMAP (0.022 g, 0.180 mmol, 0.001 equiv.) wereadded at RT and stirred for 12 h. After consumption of the startingmaterial (monitored by TLC), volatiles were removed under reducedpressure to afford compound 2a (19.6 g, 90.3%) as a brown syrup.

TLC: 50% EtOAc/Hexane (Rf: 0.40)

¹H NMR (400 MHz, CDCl₃): δ 3.74 (t, J=6.8 Hz, 2H), 2.50 (t, J=8.0 Hz,2H), 2.01 (t, J=7.6 Hz, 2H), 1.52 (s, 9H)

tert-butyl (5-(dimethoxyphosphoryl)-4-oxopentyl)carbamate (3a): To astirred solution of iPr₂NH (2.99 mL, 21.8 mmol, 1.35 equiv.) in THF,cooled to −10° C., hexyl lithium (8.79 mL, 20.0 mmol, 1.24 equiv.) wasslowly added. The reaction mixture was cooled to −60° C., dimethylmethylphosphonate (2.20 mL, 20.9 mmol, 1.29 equiv.) was added and stirred for1 h. Then the temperature was raised to −40° C., and compound 2a (3.0 g,16.2 mmol, 1.0 equiv.) was introduced to the reaction mixture andstirring was continued for further 1 h. After consumption of thestarting material, 2N H₂SO₄ solution (20 mL) was added slowly to thereaction and stirred at 0° C. for 15 minutes. The aqueous layer wasextracted with EtOAc (2×25 mL). The combined organic extracts werewashed with water (25 mL), brine (25 ml), dried over Na₂SO₄, filteredand evaporated under reduced pressure to afford compound 3a as a brownliquid (5.0 g, crude).

TLC: 80% EtOAc/Hexane (Rf: 0.30)

¹H NMR (400 MHz, CDCl₃): δ 4.85 (brs, 1H, Exc), 3.80-3.72 (m, 8H),3.13-3.07 (m, 2H), 2.67 (t, J=6.8 Hz, 2H), 1.87-1.76 (m, 2H), 1.43 (s,9H)

LC-MS: m/z=308.3 [M+H]⁺ at RT 2.67 (99.1% purity)

tert-butyl (3-(1,8-naphthyridin-2-yl)propyl)carbamate (5a): To a stirredsolution of compound 4a (0.500 g, 4.09 mmol, 1.0 equiv.) and compound 3a(1.26 g, crude, 1.0 equiv.) in MeOH (9.17 mL), 50% NaOH solution (0.314mL) was added and the reaction mixture was stirred at 50° C. for 10 h.After consumption of the starting material (by TLC), volatiles wereremoved, crude residue was diluted with EtOAc (15 mL) and the organiclayer was washed with water (2×15 mL). The separated organic layer wasdried over Na₂SO₄, filtered and concentrated under reduced pressure toafford brown syrup, which was purified by column chromatography onneutral alumina (80% EtOAc: Hexane) to provide compound 5a (0.980 g,83.3%) as an off-white solid.

TLC: EtOAc

¹H NMR (500 MHz, CDCl₃): δ 9.09 (s, 1H), 8.17-8.15 (m,1H), 8.10 (d,J=8.0 Hz, 1H), 7.45 (t, J=8.0 Hz, 1H), 7.41 (t, J=15.0, 1H), 4.76 (brs,1H, Exc), 3.25-3.21 (m, 2H), 3.09 (t, J=10.0 Hz, 2H), 2.14-2.08 (m, 2H),1.42 (s, 9H)

LC-MS: m/z=288 [M−H]⁻ at RT 2.86 (94.7%)

tert-butyl (3-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl)carbamate(S-024): To a stirred solution of compound 5a (0.25 g, 0.87 mmol, 1.00equiv.) in MeOH (5 mL), Rh/C (catalytic, 5 wt %) was added under N₂atmosphere and stirred at RT for 8 h under hydrogen (balloon pressure)atmosphere. After completion of the starting material, the reactionmixture was filtered through pad of CELITE®, washed with MeOH (5 mL).The filtrate was evaporated under reduced pressure to afford compoundS-024 (0.18 g, 71.1%) as a white solid.

TLC: EtOAc

¹H NMR (400 MHz, CDCl₃): δ 7.05 (d, J=7.6 Hz, 1H), 6.34 (d, J=7.2 Hz,1H), 5.44 (s, 1H), 4.78 (brs, 1H, Exc), 3.41-3.38 (m, 2H), 3.16 (d,J=6.0 Hz, 2H), 2.68 (t, J=6.0 Hz, 2H), 2.59 (t, J=7.6 Hz, 2H),1.93-1.81(m, 4H), 1.44 (s, 9H)

LC-MS: m/z=292.3 [M+H]⁺ at RT 3.41(97.9% purity)

3-(5, 6, 7, 8-tetrahydro-1,8-naphthyridin-2-yl)propan-1-amine (6b): To astirred solution of S-024 (0.25 g, 0.85 mmol, 1.00 equiv.) in DCM (5mL), cooled to 0° C., TFA (0.13 mL, 1.69 mmol, 2.00 equiv.) was added.The reaction was warmed to RT and stirred for 4 h. After consumption ofthe starting material (by TLC), the reaction mixture was concentratedunder reduced pressure to afford crude compound 6b (0.30 g) as a thicksyrup which was used in the next step without purification.

Synthesis of Fragment 9 and Completion of the Synthesis

5-bromo-2-(difluoromethoxy)pyridine (2): To a stirred solution ofcompound 1 (4.50 g, 25.8 mmol, 1.0 equiv.) in anhydrous MeCN (80 mL),sodium 2-chloro-2,2-difluoroacetate (4.89 g, 31.0 mmol, 1.20 equiv.) wasadded at RT and stirred at 70° C. for 48 h. After consumption of thestarting material (by TLC), the reaction mixture was brought to RT anddiluted with NH₄Cl solution (30 mL). The aqueous layer was extractedwith EtOAc (2×40 mL). The combined organic layers were washed with brinesolution (2×50 mL), dried over anhydrous Na₂SO₄, filtered andconcentrated under reduced pressure to give the crude compound which waspurified by column chromatography (2% EtOAc/hexane) to afford compound 2(3.2 g, 57%) as pale yellow syrup.

TLC: 5% EtOAc/Hexane (Rf: 0.5) z

¹H NMR (400 MHz, CDCl₃): δ 8.25 (d, J=2.8 Hz, 1H), 7.82 (dd, J=2.4, 6.4Hz, 1H), 7.40 (t, J=72.8 Hz, 1H), 6.83 (d, J=8.8 Hz, 1H)

LC-MS: m/z=224.7 [M+H]⁺ at RT 4.22 (98.2% purity)

(E)-tert-butyl 3-(6-(difluoromethoxy)pyridin-3-yl)acrylate (3): To astirred solution of tert-butyl acrylate (9.99 g, 78.1 mmol, 3.50equiv.), Et₃N (8.5 mL, 60.2 mmol, 2.70 equiv.), N-methyl pyrrolidine (20mL), Tritolylphosphine (1.17 g, 3.52 mmol, 0.16 equiv.) followed byPd(OAc)₂ (0.50 g, 2.22 mmol, 0.09 equiv.) were added. The temperaturewas gradually raised to 90° C. and compound 2 (5.00 g, 22.3 mmol, 1.0equiv.) in NMP (10 mL) was added drop wise and stirred at 90° C. for 12h. After consumption of the starting material (by TLC), the reactionmixture was filtered through pad of CELITE® and washed with EtOAc (50mL). The combined filtrate was washed with cold water (2×50 mL) followedby NaOCl (50 mL), brine solution (50 mL). The organic layer was driedover anhydrous Na₂SO₄, filtered and concentrated under reduced pressureto give the crude residue which was purified by column chromatography(3% EtOAc/hexane) to afford compound 3 (4.0 g, 66%) as yellow solid.

TLC: 5% EtOAc/Hexane (Rf: 0.5)

¹H NMR (400 MHz, CDCl₃): δ 8.28 (d, J=2.4 Hz, 1H), 7.88 (dd, J=2.0, 6.4Hz, 1H), 7.56 (d, J=16.0 Hz, 1H), 7.55 (t, J=45.6 Hz, 1H), 6.91 (d,J=8.4 Hz, 1H), 6.34 (d, J=16.0 Hz, 1H), 1.53 (s, 9H)

LC-MS: m/z=272 [M+H]⁺ at RT 4.16 (99.5% purity)

(S)-tert-butyl 3-(benzyl((R)-1-phenylethyl)amino)-3-(6-methoxypyridin-3-yl)propanoate (5): To astirred solution of compound 4 (0.39 g, 1.85 mmol, 2.0 equiv.) in THF (5mL), cooled to −30° C., n-BuLi (0.66 mL, 1.65 mmol, 1.79 equiv.) wasadded and then cooled to −78° C. Compound 3 (0.25 g, 0.92 mmol, 1.0equiv.) dissolved in THF (3 mL) was added to the reaction mixture,stirred for 30 min and quenched with saturated ammonium chloride. Thereaction mixture was extracted with EtOAc (2×20 mL). The combinedorganic extracts were washed with 10% AcOH, brine solution which wasdried over anhydrous Na₂SO₄, filtered and concentrated under reducedpressure to give the crude compound (mixture of 3 and 5, 0.17 g) asthick syrup, which was directly used in the next step.

TLC: 5% EtOAc/Hexane (Rf: 0.5)

LC-MS: m/z=483 [M+H]⁺ at RT 4.66 (75.1% purity)

Synthesis of (S)-tert-butyl3-amino-3-(6-(difluoromethoxy)pyridin-3-yl)propanoate (S-029): To astirred solution of compound 5 (0.80 g, crude mixture) in EtOAc (5 mL)and AcOH (0.5 mL), 20% Pd(OH)₂ (50 mg) was added under N₂ atmosphere.The reaction mixture was stirred under H₂ atmosphere (40 psi) at RT for2 h. After consumption of the starting material (monitored by TLC), thereaction mixture was filtered through a pad of CELITE®. Filtrate wasconcentrated under reduced pressure to afford crude compound which waspurified by column chromatography (2% MeOH/DCM) to furnish S-029 (0.3 g,63%) as yellow syrup.

TLC: 5% MeOH/DCM (Rf: 0.3)

¹H NMR (400 MHz, CDCl₃): δ 8.17 (d, J=2.8 Hz, 1H), 7.78 (dd, J=2.4, 6.4Hz, 1H), 7.44 (t, 73.2 Hz, 1H), 6.88 (d, J=8.4 Hz, 1H), 4.43-4.40 (m,1H), 2.65-2.56 (m, 2H), 1.42 (s, 9H)

LC-MS: m/z=274 [M+H]⁺ at RT 2.76 (99.8% purity)

(S, E)-tert-Butyl 3-(6-(tert-butoxy) pyridin-3-yl)-3-((2,2-dimethoxyethylidene)amino)propanoate (7): To a stirred solution ofdimethoxy acetaldehyde (0.44 mL, 2.50 mmol, 1.20 equiv., 60% in water)in DCM (10 mL), cooled to 0° C., anhydrous MgSO₄ (10 g) was addedfollowed by S-029 (600 mg, 2.08 mmol, 1.0 equiv.) in DCM (5 mL). Thereaction was continued at RT for 2 h and filtered through a pad ofCELITE®, the filtrate was concentrated under reduced pressure to affordcompound 7 (650 mg, crude) as a yellow liquid which was used in the nextstep without any purification.

TLC: 5% MeOH/DCM (Rf: 0.5)

(S)-tert-butyl 3-(6-(difluoromethoxy)pyridin-3-yl)-3-((2,2-dimethoxyethyl) amino) propanoate (8): To a stirred solution ofcompound 7 (0.65 g, crude, 1.0 equiv.) in MeOH (7 mL), cooled to 0° C.,NaBH(CN)₃ (0.13 g, 2.09 mmol, 1.20 equiv.) was added and the reactionmixture was stirred at RT for 2 h. After consumption of the startingmaterial (by TLC), MeOH was removed under reduced pressure to give thecrude residue which was diluted with water (10 mL) and extracted withEtOAc (2×10 ml). The combined organic extracts were dried over anhydrousNa₂SO₄, filtered and concentrated under reduced pressure to give thecrude material which was purified by column chromatography (2% MeOH/DCM)to afford compound 8 (0.52 g, 79%) as a thick syrup.

TLC: 5% MeOH/DCM (Rf: 0.7)

¹H NMR (400 MHz, CDCl₃): δ 8.13 (d, J=2.0 Hz, 1H), 7.75 (dd, J=2.4, 6.0Hz, 1H), 7.44 (t, J=73.2 Hz, 1H), 6.87 (d, J=8.4 Hz, 1H), 4.43-4.37 (m,2H), 4.06-4.02 (m, 1H), 3.60-3.54 (m, 2H), 3.35 (s, 3H) 3.31 (s, 3H),2.66-2.57 (m, 2H), 1.39 (s, 9H)

LC-MS: m/z=377 [M+H]⁺ at RT 2.96 (92.3% purity)

(S)-tert-butyl 3-(6-(difluoromethoxy) pyridin-3-yl)-3-(1-(2,2-dimethoxyethyl)-3-(3-(5, 6, 7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl)ureido)propanoate (10): To astirred solution of compound 8 (375 mg, 0.99 mmol, 1.0 equiv.) in dryDCM (5 mL), cooled to 0° C., triphosgene (1.50 mL, 2.99 mmol, 3.00equiv., 20% in PhMe) followed by Et₃N (0.30 mL, 2.09 mmol, 2.10 equiv)were added. The reaction mixture was slowly brought to RT and stirredfor 2 h. After completion of the starting material, volatiles wereevaporated to afford the crude compound 9, which was used directly inthe next step without purification. A solution of compound 9 in DCE (2mL) was added to a solution of compound 6b (400 mg, 1.32 mmol, 1.32equiv.) in DCM (5 mL), Et₃N (0.55 mL, 3.98 mmol, 4.00 equiv) at 0° C.and stirred at RT for 4 h. After consumption of the starting material(monitored by TLC), the reaction mixture was concentrated under reducedpressure to give the crude residue which was purified by columnchromatography (2% MeOH/DCM) to afford compound 10 (0.40 g, 67%) as athick syrup.

TLC: 5% MeOH/DCM (Rf: 0.2)

¹H NMR (400 MHz, CDCl₃): δ 8.13 (d, J=2.8 Hz, 1H), 7.79 (dd, J=2.4, 6.4Hz, 1H), 7.62 (tt, J=72.8 Hz, 1H), 7.12 (d, J=6.4 Hz, 1H), 6.86 (d,J=8.4 Hz, 1H), 6.36 (d, J=3.6 Hz, 1H), 6.22 (t, J=4.8 Hz, 1H), 5.75 (t,J=7.6 Hz, 1H), 4.26 (t, J=5.2 Hz, 1H), 3.45-3.38 (m, 8H), 3.27-3.13 (m,3H), 2.99-2.93 (m, 2H), 2.71-2.59 (m, 5H), 1.93-1.83 (m, 5H), 1.39 (s,9H)

LC-MS: m/z=594 [M+H]⁺ at RT 3.42 (88.1% purity)

(S)-tert-Butyl 3-(6-(difluoromethoxy) pyridin-3-yl)-3-(2-oxo-3-(3-(5, 6,7, 8-tetrahydro-1,8-naphthyridin-2-yl)propyl)-2,3-dihydro-1H-imidazol-1-yl)propanoate (11): To a stirred solution ofcompound 10 (0.20 g, 0.34 mmol, 1.0 equiv.) in THF (4 mL), at −10° C., 1M sulfuric acid (0.8 mL) was added. The reaction was slowly warmed to RTand stirred for 10 h. After consumption of the starting material(monitored by LCMS), THF was removed and the crude residue wasneutralized with sodium hydroxide (50 wt %) till pH ˜7. The aqueouslayer was extracted with 5% MeOH/DCM (3×20 mL) and the combined organicextracts were dried over anhydrous Na₂SO₄, filtered and concentratedunder reduced pressure to furnish compound 11 (0.22 g, crude) as asyrup.

TLC: 10% MeOH/DCM (Rf: 0.5)

LC-MS: m/z=530 [M+H]⁺ at RT 4.06 (72.8% purity)

(S)-tert-Butyl 3-(6-(difluoromethoxy) pyridin-3-yl)-3-(2-oxo-3-(3-(5, 6,7, 8-tetrahydro-1,8-naphthyridin-2-yl)propyl)imidazolidin-1-yl)propanoate (12): To a stirred solution of compound 11(0.45 g, crude, 1.0 equiv.) in EtOH (8 mL), 20% Pd/C (200 mg) was addedunder N₂ atmosphere. The reaction mixture was stirred under H₂atmosphere (40 psi) at RT for 36 h. After consumption of the startingmaterial the reaction mixture was filtered through a pad of CELITE®, andthe filtrate was concentrated under reduced pressure to afford crudecompound 12, which was purified by chiral preparative HPLC to affordcompound 12 (450 mg, crude) as an off-white solid.

TLC: 10% MeOH/DCM (Rf: 0.5)

LC-MS: m/z=532.6 [M+H]⁺ at RT 3.99 (80.1% purity)

(S)-3-(6-(difluoromethoxy)pyridin-3-yl)-3-(2-oxo-3-(3-(5, 6, 7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl) imidazolidin-1-yl)propanoicacid (Compound A1): To a stirred solution of compound 12 (0.40 g, crude,1.0 equiv.) in DCM (2 mL), cooled to −10° C., TFA (0.5 mL) was addedunder N₂ atmosphere. The reaction was slowly brought to RT and stirredfor 2 h; after consumption of the starting material, volatiles wereevaporated to afford crude (400 mg) compound, which was purified bychiral preparative HPLC to afford compound A1 as an off-white solid.

TLC: 10% MeOH/DCM (Rf: 0.3) ¹H NMR (400 MHz, CD₃OD): δ 8.20 (d, J=2.4Hz, 1H), 7.85 (dd, J=2.4, 6.4 Hz, 1H), 7.53 (t, J=2.4 Hz, 1H), 7.50 (d,J=7.2 Hz, 1H), 6.98 (d, J=8.4 Hz, 1H), 6.57 (d, J=7.2 Hz, 1H), 5.51 (dd,J=3.6, 8.0 Hz, 1H), 3.68-3.61 (m, 1H), 3.52-3.46 (m, 3H), 3.38 (m, 1H),3.24-3.17 (m, 1H), 3.07-2.98 (m, 2H), 2.90-2.62 (m, 6H), 2.09-1.81 (m,4H).

LC-MS: m/z=476 [M+H]⁺ at RT 2.78 (97.9% purity)

HPLC purity: 96.4%; Chiral Purity: 99%

The compounds of the present invention described in Examples 2-7 inwhich Z is —CH₂CH₂CH₂— were synthesized using the general reactionscheme shown in Scheme 2. Dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate wasadded to the fluorinated nitrogen heterocycle (Q) aldehyde to form thehept-1-en-3-one. The hept-1-en-3-one was reduced to the correspondinghept-1-en-3-ol using lithium aluminum hydride or sodium borohydride. Thehept-1-en-3ol was then reacted with proprionic acid in1,1,1-triethoxyethane and the resulting crude rearrangement product wasreduced with hydrogen and palladium on carbon catalyst to thecorresponding olefin reduction product which was then reacted withaqueous base to form the final nonanoic acid compounds.

Example 2 Synthesis of9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-3-(2-(trifluoromethyl)pyrimidin-5-yl)nonanoicacid (Compound A2)(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)hept-1-en-3-one

Under nitrogen, to dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate(3.40 g, 10.0 mmol, 1.00 equiv; Coleman, P. J. et al., J. Med. Chem.2004, 47:4829-4837) in THF (10 mL) at 23° C. was added2-(trifluoromethyl)pyrimidine-5-carbaldehyde (1.76 g, 10.0 mmol, 1.00equiv) and t-BuOK (1.01 g, 9.00 mmol, 0.900 equiv). After stirring for10 min at 23° C., the reaction mixture was directly loaded on silica geland purified by column chromatography on silica gel eluting withCH₂Cl₂/MeOH to afford 2.10 g of the title compound (54% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 9.03 (s, 2H), 7.50 (d, J=16.2 Hz,1H), 7.07 (d, J=7.2 Hz, 1H), 6.93 (d, J=16.2 Hz, 1H), 6.35 (d, J=7.2 Hz,1H), 5.17 (br s, 1H), 3.42-3.37 (m, 2H), 2.79-2.64 (m, 4H), 2.62-2.55(m, 2H), 1.95-1.85 (m, 2H), 1.77-1.66 (m, 4H). ¹⁹F NMR (282 MHz, CDCl₃,23° C., δ): −70.3 (s, 3F).

(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)hept-1-en-3-ol

Under nitrogen, to(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)hept-1-en-3-one(1.20 g, 3.07 mmol, 1.00 equiv) in THF (15 mL) at −78° C. was addedLiAlH₄ (1.0 M in THF, 3.07 mL, 3.07 mmol, 1.00 equiv). After stirringfor 10 min at −78° C., H₂O (116 μL), 15% NaOH aq (116 μL) and H₂O (348μL) were added sequentially to the reaction mixture. The reactionmixture was warmed to 23° C. and filtered through a pad of CELITE®. Thefiltrate was concentrated in vacuo and the residue was purified bycolumn chromatography on silica gel eluting with CH₂Cl₂/MeOH to afford560 mg of the title compound (46% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.86 (s, 2H), 7.06 (d, J=7.2 Hz,1H), 6.66 (d, J=16.2 Hz, 1H), 6.53 (dd, J=16.2 Hz, 4.5 Hz, 1H), 6.34 (d,J=7.2 Hz, 1H), 4.81 (br s, 1H), 4.50-4.40 (m, 1H), 3.42-3.37 (m, 2H),2.70-2.50 (m, 4H), 1.96-1.40 (m, 8H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C.,δ): −70.1 (s, 3F).

9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-3-(2-(trifluoromethyl)pyrimidin-5-yl)nonanoicacid (Compound A2)

Under nitrogen, to(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)hept-1-en-3-ol(560 mg, 1.43 mmol, 1.00 equiv) in MeC(OEt)₃ (14 mL) at 23° C. was addedEtCO2H (107 μL, 1.43 mmol, 1.00 equiv). After stirring for 2 hr at 140°C., the reaction mixture was directly loaded on silica gel and purifiedby column chromatography on silica gel eluting with hexanes/EtOAc toafford a crude rearrangement product, which was used in the next stepwithout further purification.

Under air, to the above obtained residue in MeOH-TFA (10 mL-1 mL) at 23°C. was added 10% Pd/C (103 mg, 0.0969 mmol, 6.78 mol %) and H₂ wasintroduced with a balloon. After stirring for 1 hr at 23° C., thereaction mixture was filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo to afford a crude olefin reduction product, whichwas used in the next step without further purification.

Under air, to the above obtained residue in MeOH (10 mL) at 23° C. wasadded 15% NaOH aq (2.7 mL). After stirring for 20 min at 60° C., thereaction mixture was neutralized with 3N HCl and concentrated in vacuoto remove MeOH. The residual aqueous solution was extracted with EtOAc(3×10 mL) and the combined organic phases were washed with NaHCO₃ aq(2×5 mL) and dried (MgSO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography on silica gel elutingwith CH₂Cl₂/MeOH to afford 280 mg of the title compound (45% yield over3 steps).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.79 (s, 2H), 7.24 (d, J=7.2 Hz,1H), 6.25 (d, J=7.2 Hz, 1H), 3.48-3.40 (m, 2H), 3.38-3.32 (m, 1H),2.75-2.52 (m, 4H), 1.95-1.80 (m, 4H), 1.75-1.58 (m, 4H), 1.40-1.18 (m,6H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −70.1 (s, 3F).

Example 3 Synthesis of3-(6-(difluoromethoxy)pyridin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A3) 6-(difluoromethoxy)nicotinaldehyde

Under nitrogen, to 5-bromo-2-(difluoromethoxy)pyridine (448 mg, 2.00mmol, 1.00 equiv; Ando, M. et al., Org. Lett. 2006, 8:3805-3808) in THF(10 mL) at −78° C. was added t-BuLi (1.7 M in pentane, 2.35 mL, 4.00mmol, 2.00 equiv) dropwise over 5 min. After stirring for 20 min at −78°C., DMF (0.54 mL, 7.0 mmol, 3.5 equiv) was added to the reactionmixture. After stirring for 20 min at −78° C., 1N HCl aq (10 mL) wasadded to the reaction mixture and the reaction mixture was warmed to 23°C. The phases were separated and the aqueous phase was extracted withEtOAc (3×5 mL). The combined organic phases were washed with brine (10mL) and dried (MgSO₄). The filtrate was concentrated in vacuo and theresidue was purified by column chromatography on silica gel eluting withhexanes/EtOAc to afford 105 mg of the title compound (30% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 10.05 (s, 1H), 8.69 (d, J=2.1 Hz,1H), 8.24 (dd, J=8.4 Hz, 2.4 Hz, 1H), 7.56 (t, J=72.3 Hz, 1H), 7.04 (d,J=8.4 Hz, 1H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −89.8 (d, J=72.3 Hz,2F).

(E)-1-(6-(difluoromethoxy)pyridin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one

Under nitrogen, to dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate(1.57 g, 4.62 mmol, 1.00 equiv) in MeCN (11 mL) at 23° C. was added6-(difluoromethoxy)nicotinaldehyde (800 mg, 4.62 mmol, 1.00 equiv), LiCl(196 mg, 4.62 mmol, 1.00 equiv) and DBU (0.725 mL, 4.85 mmol, 1.05equiv). After stirring for 1 hr at 50° C., the reaction mixture wascooled to 23° C. and was filtered through a pad of CELITE®. The filtratewas concentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 1.27 gof the title compound (71% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.32 (d, J=2.4 Hz, 1H), 7.92 (dd,J=8.4 Hz, 2.4 Hz, 1H), 7.49 (t, J=72.3 Hz, 1H), 7.47 (d, J=16.2 Hz, 1H),7.06 (d, J=7.2 Hz, 1H), 6.93 (d, J=8.7 Hz, 1H), 6.70 (d, J=16.2 Hz, 1H),6.35 (d, J=7.2 Hz, 1H), 4.89 (br s, 1H), 3.42-3.36 (m, 2H), 2.76-2.64(m, 4H), 2.62-2.56 (m, 2H), 1.94-1.85 (m, 2H), 1.80-1.66 (m, 4H). ¹⁹FNMR (282 MHz, CDCl₃, 23° C., δ): −89.2 (d, J=72.3 Hz, 2F).

(E)-1-(6-(difluoromethoxy)pyridin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol

Under nitrogen, to(E)-1-(6-(difluoromethoxy)pyridin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one(1.27 g, 3.28 mmol, 1.00 equiv) in THF (33 mL) at 0° C. was added LiAlH₄(1.0 M in THF, 3.28 mL, 3.28 mmol, 1.00 equiv). After stirring for 10min at 0° C., H₂O (124 μL), 15% NaOH aq (124 μL) and H₂O (372 μL) wereadded sequentially to the reaction mixture. The reaction mixture waswarmed to 23° C. and filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 1.05 gof the title compound (82% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.22 (d, J=2.4 Hz, 1H), 7.84 (dd,J=8.4 Hz, 2.4 Hz, 1H), 7.49 (t, J=72.3 Hz, 1H), 7.05 (d, J=7.2 Hz, 1H),6.88 (d, J=8.7 Hz, 1H), 6.66 (d, J =16.2 Hz, 1H), 6.55 (dd, J=16.2 Hz,4.5 Hz, 1H), 6.33 (d, J=7.2 Hz, 1H), 4.84 (br s, 1H), 4.52-4.43 (m, 1H),3.40-3.37 (m, 2H), 2.72-2.51 (m, 4H), 1.95-1.40 (m, 8H). ¹⁹F NMR (282MHz, CDCl₃, 23° C., δ): −89.0 (d, J=72.5 Hz, 2F).

3-(6-(difluoromethoxy)pyridin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A3)

Under nitrogen, to(E)-1-(6-(difluoromethoxy)pyridin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol(1.05 g, 2.70 mmol, 1.00 equiv) in MeC(OEt)₃ (27 mL) at 23° C. was addedEtCO₂H (201 μL, 2.70 mmol, 1.00 equiv). After stirring for 2 hr at 140°C., the reaction mixture was directly loaded on silica gel and purifiedby column chromatography on silica gel eluting with hexanes/EtOAc toafford a crude rearrangement product, which was used in the next stepwithout further purification.

Under air, to the above obtained residue in MeOH-TFA (10 mL-1 mL) at 23°C. was added 10% Pd/C (176 mg, 0.165 mmol, 6.11 mol %) and H₂ wasintroduced with a balloon. After stirring for 1 hr at 23° C., thereaction mixture was filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo to afford a crude olefin reduction product, whichwas used in the next step without further purification.

Under air, to the above obtained residue in MeOH (10 mL) at 23° C. wasadded 15% NaOH aq (4.4 mL). After stirring for 20 min at 60° C., thereaction mixture was neutralized with 3N HCl and concentrated in vacuoto remove MeOH. The residual aqueous solution was extracted with EtOAc(3×10 mL) and the combined organic phases were washed with NaHCO₃ aq(2×5 mL) and dried (MgSO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography on silica gel elutingwith CH₂Cl₂/MeOH to afford 400 mg of the title compound (34% yield over3 steps).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.06 (d, J=2.4 Hz, 1H), 7.66 (dd,J=8.4 Hz, 2.4 Hz, 1H), 7.43 (t, J=72.3 Hz, 1H), 7.20 (d, J=8.7 Hz, 1H),6.84 (d, J=7.2 Hz, 1H), 6.25 (d, J=7.2 Hz, 1H), 3.46-3.40 (m, 2H),3.38-3.28 (m, 1H), 2.79-2.40 (m, 4H), 1.95-1.80 (m, 4H), 1.75-1.62 (m,4H), 1.40-1.20 (m, 6H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −88.3 (d,J=72.5 Hz, 2F).

Example 4 Synthesis of3-(6-fluoroquinolin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A4) 6-fluoroquinoline-3-carbaldehyde

Under nitrogen, to 2-chloro-6-fluoroquinoline-3-carbaldehyde (2.03 g,9.68 mmol, 1.00 equiv) in DMF (10 mL) at 23° C. was added triethylamine(16.2 mL, 116 mmol, 12.0 equiv), Pd(PPh₃)₄ (559 mg, 0.484 mmol, 5.00 mol%), and formic aid (1.29 mL, 34.2 mmol, 5.40 equiv). After stirring for1 hr at 100° C., the reaction mixture was cooled to 23° C. and water (40mL) and EtOAc (30 mL) was added. The phases were separated and theaqueous phase was extracted with EtOAc (3×30 mL). The combined organicphases were washed with brine (50 mL) and dried (MgSO₄). The filtratewas concentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with hexanes/EtOAc to afford 734 mgof the title compound (43% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 10.27 (s, 1H), 9.34 (d, J=2.1 Hz,1H), 8.60 (d, J=1.8 Hz, 1H), 8.21 (dd, J=9.0 Hz, 4.8 Hz, 1H), 7.70-7.60(m, 2H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −110.8 (m, 1F).

(E)-1-(6-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one

Under nitrogen, to dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate(900 mg, 2.64 mmol, 1.10 equiv) in MeCN (22 mL) at 23° C. was added6-fluoroquinoline-3-carbaldehyde (420 mg, 2.40 mmol, 1.00 equiv), LiCl(101 mg, 2.40 mmol, 1.00 equiv) and DBU (0.377 mL, 2.52 mmol, 1.05equiv). After stirring for 1 hr at 75° C., the reaction mixture wascooled to 23° C. and was filtered through a pad of CELITE®. The filtratewas concentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 900 mgof the title compound (96% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 9.06 (d, J=2.4 Hz, 1H), 8.21 (d,J=2.1 Hz, 1H), 8.11 (dd, J=10.6 Hz, 5.7 Hz, 1H), 7.66 (d, J=16.2 Hz,1H), 7.58-7.43 (m, 2H), 7.06 (d, J=7.2 Hz, 1H), 6.96 (d, J=16.2 Hz, 1H),6.37 (d, J=7.2 Hz, 1H), 4.76 (br s, 1H), 3.43-3.35 (m, 2H), 2.78-2.65(m, 4H), 2.63-2.56 (m, 2H), 1.94-1.85 (m, 2H), 1.82-1.66 (m, 4H). ¹⁹FNMR (282 MHz, CDCl₃, 23° C., δ): −111.9 (m, 1F).

(E)-1-(6-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol

Under air, to(E)-1-(6-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one(490 mg, 1.26 mmol, 1.00 equiv) in MeOH (29 mL) at 0° C. was added NaBH₄(71.5 mg, 1.89 mmol, 1.5 equiv). After stirring for 1 hr at 0° C., 1NHCl aq (10 mL) was added to the reaction mixture and concentrated invacuo to remove MeOH. The residue was neutralized with NaHCO₃ aq andEtOAc (10 mL) was added. The phases were separated and the aqueous phasewas extracted with EtOAc (3×20 mL). The combined organic phases werewashed with brine (30 mL) and dried (MgSO₄). The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 490 mgof the title compound (99% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.95 (s, 1H), 8.06 (dd, J=10.6 Hz,5.7 Hz, 1H), 7.99 (s, 1H), 7.50-7.40 (m, 2H), 7.06 (d, J=7.2 Hz, 1H),6.75 (d, J=16.2 Hz, 1H), 6.49 (dd, J=16.2 Hz, 4.5 Hz, 1H), 6.34 (d,J=7.2 Hz, 1H), 4.94 (br s, 1H), 4.47-4.39 (m, 1H), 3.42-3.38 (m, 2H),2.70-2.47 (m, 4H), 1.96-1.45 (m, 8H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C.,δ): −111.8 (m, 1F).

3-(6-fluoroquinolin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A4)

Under nitrogen, to(E)-1-(6-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol(489 mg, 1.25 mmol, 1.00 equiv) in MeC(OEt)₃ (12 mL) at 23° C. was addedEtCO₂H (93.3 μL, 1.25 mmol, 1.00 equiv). After stirring for 2 hr at 140°C., the reaction mixture was directly loaded on silica gel and purifiedby column chromatography on silica gel eluting with hexanes/EtOAc toafford a crude rearrangement product, which was used in the next stepwithout further purification.

Under air, to the above obtained residue in MeOH-TFA (10 mL-1 mL) at 23°C. was added 10% Pd/C (128 mg, 0.121 mmol, 9.68 mol %) and H₂ wasintroduced with a balloon. After stirring for 1 hr at 23° C., thereaction mixture was filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo to afford a crude olefin reduction product, whichwas used in the next step without further purification.

Under air, to the above obtained residue in MeOH (10 mL) at 23° C. wasadded 15% NaOH aq (3.0 mL). After stirring for 20 min at 60° C., thereaction mixture was neutralized with 3N HCl and concentrated in vacuoto remove MeOH. The residual aqueous solution was extracted with EtOAc(3×10 mL) and the combined organic phases were washed with NaHCO₃ aq(2×5 mL) and dried (MgSO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography on silica gel elutingwith CH₂Cl₂/MeOH to afford 500 mg of the title compound (92% yield over3 steps).

¹H NMR (300 MHz, CD₃OD, 23° C., δ): 8.78 (s, 1H), 8.11 (s, 1H),8.00-7.93 (m, 1H), 7.52-7.42 (m, 2H), 7.31 (d, J=7.2 Hz, 1H), 6.35 (d,J=7.2 Hz, 1H), 3.38-3.20 (m, 3H), 2.77-2.42 (m, 4H), 1.90-1.20 (m, 14H).¹⁹F NMR (282 MHz, CD₃OD, 23° C., δ): −110.9 (m, 1F).

Example 5 Synthesis of3-(7-fluoroquinolin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A5)(E)-1-(7-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one

Under nitrogen, to dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate(749 mg, 2.20 mmol, 1.10 equiv) in MeCN (22 mL) at 23° C. was added7-fluoroquinoline-3-carbaldehyde (350 mg, 2.00 mmol, 1.00 equiv; Sato,I. et al., Synthesis 2004, 9:1419-1428), LiCl (84.8 mg, 2.00 mmol, 1.00equiv) and DBU (0.314 mL, 2.10 mmol, 1.05 equiv). After stirring for 1hr at 75° C., the reaction mixture was cooled to 23° C. and was filteredthrough a pad of CELITE®. The filtrate was concentrated in vacuo and theresidue was purified by column chromatography on silica gel eluting withCH₂Cl₂/MeOH to afford 570 mg of the title compound (73% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 9.10 (d, J=2.4 Hz, 1H), 8.28 (d,J=2.1 Hz, 1H), 7.87 (dd, J=9.0 Hz, 6.0 Hz, 1H), 7.74 (dd, J=9.9 Hz, 2.4Hz, 1H), 7.69 (d, J=16.2 Hz, 1H), 7.42-7.33 (m, 1H), 7.11 (d, J=7.2 Hz,1H), 6.94 (d, J=16.2 Hz, 1H), 6.37 (d, J=7.2 Hz, 1H), 5.41 (br s, 1H),3.43-3.37 (m, 2H), 2.78-2.58 (m, 6H), 1.93-1.85 (m, 2H), 1.81-1.69(m,4H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −107.0 (m, 1F).

(E)-1-(7-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol

Under air, to(E)-1-(7-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one(300 mg, 0.770 mmol, 1.00 equiv) in MeOH (8 mL) at 0° C. was added NaBH₄(87.4 mg, 2.31 mmol, 3.00 equiv). After stirring for 30 min at 0° C., 1NHCl aq (10 mL) was added to the reaction mixture and concentrated invacuo to remove MeOH. The residue was neutralized with NaHCO₃ aq andEtOAc (10 mL) was added. The phases were separated and the aqueous phasewas extracted with EtOAc (3×20 mL). The combined organic phases werewashed with brine (30 mL) and dried (MgSO₄). The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 210 mgof the title compound (70% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.98 (s, 1H), 8.07 (s, 1H), 7.81(dd, J=9.0 Hz, 6.0 Hz, 1H), 7.78 (dd, J=9.9 Hz, 2.4 Hz, 1H), 7.63 (br s,1H), 7.39-7.28 (m, 1H), 6.78 (d, J=16.2 Hz, 1H), 6.47 (dd, J=16.2 Hz,4.5 Hz, 1H), 6.36 (d, J=7.2 Hz, 1H), 4.48-4.41 (m, 1H), 3.48-3.41 (m,2H), 2.79-2.67 (m, 4H), 1.97-1.48 (m, 8H). ¹⁹F NMR (282 MHz, CDCl₃, 23°C., δ): −109.9 (m, 1F).

3-(7-fluoroquinolin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A5)

Under nitrogen, to(E)-1-(7-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol(730 mg, 1.71 mmol, 1.00 equiv) in MeC(OEt)₃ (17 mL) at 23° C. was addedEtCO₂H (128 μL, 1.71 mmol, 1.00 equiv). After stirring for 2 hr at 140°C., the reaction mixture was directly loaded on silica gel and purifiedby column chromatography on silica gel eluting with hexanes/EtOAc toafford a crude rearrangement product, which was used in the next stepwithout further purification.

Under air, to the above obtained residue in MeOH-TFA (10 mL-1 mL) at 23°C. was added 10% Pd/C (125 mg, 0.117 mmol, 6.84 mol %) and H₂ wasintroduced with a balloon. After stirring for 1 hr at 23° C., thereaction mixture was filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo to afford a crude olefin reduction product, whichwas used in the next step without further purification.

Under air, to the above obtained residue in MeOH (10 mL) at 23° C. wasadded 15% NaOH aq (3.0 mL). After stirring for 20 min at 60° C., thereaction mixture was neutralized with 3N HCl and concentrated in vacuoto remove MeOH. The residual aqueous solution was extracted with EtOAc(3×10 mL) and the combined organic phases were washed with NaHCO3 aq(2×5 mL) and dried (MgSO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography on silica gel elutingwith CH₂Cl₂/MeOH to afford 480 mg of the title compound (64% yield over3 steps).

¹H NMR (300 MHz, CD₃OD, 23° C., δ): 8.79 (s, 1H), 8.21 (s, 1H),8.00-7.91 (m, 1H), 7.62-7.57 (m, 1H), 7.48-7.38 (m, 2H), 6.47 (d, J=7.2Hz, 1H), 3.48-3.30 (m, 3H), 2.80-2.52 (m, 4H), 1.90-1.20 (m, 14H). ¹⁹FNMR (282 MHz, CD₃OD, 23° C., δ): −111.9 (m, 1F).

Example 6 Synthesis of3-(6,7-difluoroquinolin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A6) 6,7-difluoroquinoline-3-carbaldehyde

Under nitrogen, to 2-chloro-6,7-difluoroquinoline-3-carbaldehyde (1.44g, 6.33 mmol, 1.00 equiv) in DMF (6.3 mL) at 23° C. was addedtriethylamine (10.6 mL, 76.0 mmol, 12.0 equiv), Pd(PPh₃)₄ (366 mg, 0.317mmol, 5.00 mol %), and formic acid (1.29 mL, 34.2 mmol, 5.40 equiv).After stirring for 1 hr at 100° C., the reaction mixture was cooled to23° C. and water (30 mL) and EtOAc (20 mL) was added. The phases wereseparated and the aqueous phase was extracted with EtOAc (3×20 mL). Thecombined organic phases were washed with brine (50 mL) and dried(MgSO₄). The filtrate was concentrated in vacuo and the residue waspurified by column chromatography on silica gel eluting withhexanes/EtOAc to afford 500 mg of the title compound (41% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 10.26 (s, 1H), 9.35 (d, J=1.2 Hz,1H), 8.60 (d, J=1.5 Hz, 1H), 7.97 (dd, J=10.8 Hz, 7.5 Hz, 1H), 7.97 (dd,J=9.0 Hz, 8.7 Hz, 1H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −125.3 (m,1F), −132.3 (m, 1F).

(E)-1-(6,7-difluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one

Under nitrogen, to dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate(599 mg, 1.76 mmol, 1.10 equiv) in MeCN (5 mL) at 23° C. was added6,7-difluoroquinoline-3-carbaldehyde (310 mg, 1.60 mmol, 1.00 equiv),LiCl (67.8 mg, 1.60 mmol, 1.00 equiv) and DBU (0.251 mL, 1.68 mmol, 1.05equiv). After stirring for 1 hr at 75° C., the reaction mixture wascooled to 23° C. and was filtered through a pad of CELITE®. The filtratewas concentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 570 mgof the title compound (84% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 9.07 (d, J=2.4 Hz, 1H), 8.20 (d,J=2.1 Hz, 1H), 7.87 (dd, J=10.8 Hz, 7.5 Hz, 1H), 7.66 (d, J=16.2 Hz,1H), 7.62-7.53 (m, 1H), 7.06 (d, J=7.2 Hz, 1H), 6.93 (d, J=16.2 Hz, 1H),6.36 (d, J=7.2 Hz, 1H), 4.77 (br s, 1H), 3.43-3.38 (m, 2H), 2.79-2.58(m, 6H), 1.96-1.85 (m, 2H), 1.81-1.69 (m, 4H). ¹⁹F NMR (282 MHz, CDCl₃,23° C., δ): −129.1 (m, 1F), −133.6 (m, 1F).

(E)-1-(6,7-difluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol

Under nitrogen, to(E)-1-(6,7-difluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-one(1.03 g, 2.53 mmol, 1.00 equiv) in THF (25 mL) at 0° C. was added LiAlH₄(1.0 M in THF, 2.53 mL, 2.53 mmol, 1.00 equiv). After stirring for 10min at 0° C., H₂O (96 μL), 15% NaOH aq (96 μL) and H₂O (288 μL) wereadded sequentially to the reaction mixture. The reaction mixture waswarmed to 23° C. and filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 780 mgof the title compound (75% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.95 (d, J=2.4 Hz, 1H), 8.00 (d,J=2.1 Hz, 1H), 7.81 (dd, J=10.8 Hz, 7.5 Hz, 1H), 7.52 (d, J=16.2 Hz,1H), 7.21 (d, J=7.2 Hz, 1H), 6.76 (d, J =16.2 Hz, 1H), 6.48 (dd, J=16.2Hz, 4.5 Hz, 1H), 6.34 (d, J=7.2 Hz, 1H), 4.48-4.42 (m, 1H), 3.47-3.41(m, 2H), 2.79-2.67 (m, 4H), 1.97-1.47 (m, 8H). ¹⁹F NMR (282 MHz, CDCl₃,23° C., δ): −132.1 (m, 1F), −135.1 (m, 1F).

3-(6,7-difluoroquinolin-3-yl)-9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)nonanoicacid (Compound A6)

Under nitrogen, to(E)-1-(6,7-difluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol(780 mg, 1.90 mmol, 1.00 equiv) in MeC(OEt)₃ (19 mL) at 23° C. was addedEtCO₂H (142 μL, 1.90 mmol, 1.00 equiv). After stirring for 2 hr at 140°C., the reaction mixture was directly loaded on silica gel and purifiedby column chromatography on silica gel eluting with hexanes/EtOAc toafford a crude rearrangement product, which was used in the next stepwithout further purification.

Under air, to the above obtained residue in MeOH-TFA (10 mL-1 mL) at 23°C. was added 10% Pd/C (127 mg, 0.119 mmol, 6.26 mol %) and H₂ wasintroduced with a balloon. After stirring for 1 hr at 23° C., thereaction mixture was filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo to afford a crude olefin reduction product, whichwas used in the next step without further purification.

Under air, to the above obtained residue in MeOH (10 mL) at 23° C. wasadded 15% NaOH aq (3.2 mL). After stirring for 20 min at 60° C., thereaction mixture was neutralized with 3N HCl and concentrated in vacuoto remove MeOH. The residual aqueous solution was extracted with EtOAc(3×10 mL) and the combined organic phases were washed with NaHCO₃ aq(2×5 mL) and dried (MgSO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography on silica gel elutingwith CH₂Cl₂/MeOH to afford 500 mg of the title compound (58% yield over3 steps).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.79 (s, 1H), 7.97 (s, 1H),7.90-7.81 (m, 1H), 7.58-7.47 (m, 1H), 7.24 (d, J=7.2 Hz, 1H), 6.23 (d,J=7.2 Hz, 1H), 3.48-3.32 (m, 3H), 2.80-2.57 (m, 4H), 1.95-1.20 (m, 14H).¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −132.3 (m, 1F), −135.5 (m, 1F).

Example 7 Synthesis of9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-3-(7-(trifluoromethyl)quinolin-3-yl)nonanoicacid (Compound A7) 2-chloro-7-iodoquinoline-3-carbaldehyde

Under nitrogen, to POCl₃ (14.9 mL, 160 mmol, 7.00 equiv) at 0° C. wasadded DMF (4.40 mL, 57.1 mmol, 2.50 equiv). After stirring for 10 min at0° C., N-(3-iodophenyl)acetamide (5.96 g, 22.8 mmol, 1.00 equiv; Pialat,A. et al., Org. Lett. 2013, 15:1764-1767) was added to the reactionmixture. After stirring for 17 hr at 75° C., the reaction mixture waspoured into iced. The phases were separated and the aqueous phase wasextracted with CH₂Cl₂ (3×50 mL). The combined organic phases were washedwith brine (100 mL) and dried (MgSO₄). The filtrate was concentrated invacuo and the residue was purified by column chromatography on silicagel eluting with CH₂Cl₂/MeOH to afford 2.9 g of the title compound (40%yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 10.55 (s, 1H), 8.72 (s, 1H), 8.52(s, 1H), 7.93 (dd, J=8.4 Hz, 1.5 Hz, 1H), 7.69 (d, J=8.4 Hz, 1H).

2-chloro-7-(trifluoromethyl)quinoline-3-carbaldehyde

Under nitrogen, to 2-chloro-7-iodoquinoline-3-carbaldehyde (2.90 g, 9.13mmol, 1.00 equiv) in DMF (18 mL) at 23° C. was added CuI (4.35 g, 22.8mmol, 2.50 equiv) and FSO₂CF₂CO₂Me (11.6 mL, 91.3 mmol, 10.0 equiv).After stirring for 2 hr at 95° C., the reaction mixture was cooled to23° C. and filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with hexanes/EtOAc to afford 1.5 gof the title compound (63% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 10.60 (s, 1H), 8.82 (s, 1H), 8.39(s, 1H), 8.14 (d, J=8.4 Hz, 1H), 7.84 (d, J=8.4 Hz, 1H). ¹⁹F NMR (282MHz, CDCl₃, 23° C., δ): −63.2 (s, 3F).

7-(trifluoromethyl)quinoline-3-carbaldehyde

Under nitrogen, to 2-chloro-7-(trifluoromethyl)quinoline-3-carbaldehyde(1.50 g, 5.78 mmol, 1.00 equiv) in DMF (5.8 mL) at 23° C. was addedtriethylamine (9.67 mL, 69.4 mmol, 12.0 equiv), Pd(PPh₃)₄ (334 mg, 0.289mmol, 5.00 mol %), and formic aid (1.18 mL, 31.2 mmol, 5.40 equiv).After stirring for 1 hr at 100° C., the reaction mixture was cooled to23° C. and water (30 mL) and EtOAc (20 mL) was added. The phases wereseparated and the aqueous phase was extracted with EtOAc (3×20 mL). Thecombined organic phases were washed with brine (50 mL) and dried(MgSO₄). The filtrate was concentrated in vacuo and the residue waspurified by column chromatography on silica gel eluting withhexanes/EtOAc to afford 412 mg of the title compound (32% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 10.32 (s, 1H), 9.48 (d, J=1.5 Hz,1H), 8.71 (d, J=1.5 Hz, 1H), 8.51 (s, 1H), 8.15 (d, J=8.4 Hz, 1H), 7.86(d, J=8.4 Hz, 1H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −63.1 (s, 3F).

(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(7-(trifluoromethyl)quinolin-3-yl)hept-1-en-3-one

Under nitrogen, to dimethyl(2-oxo-6-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hexyl)phosphonate(685 mg, 2.01 mmol, 1.10 equiv) in MeCN (9 mL) at 23° C. was added7-(trifluoromethyl)quinoline-3-carbaldehyde (412 mg, 1.83 mmol, 1.00equiv), LiCl (77.6 mg, 1.83 mmol, 1.00 equiv) and DBU (0.287 mL, 1.92mmol, 1.05 equiv). After stirring for 1 hr at 75° C., the reactionmixture was cooled to 23° C. and was filtered through a pad of CELITE®.The filtrate was concentrated in vacuo and the residue was purified bycolumn chromatography on silica gel eluting with CH₂Cl₂/MeOH to afford706 mg of the title compound (88% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 9.19 (d, J=2.4 Hz, 1H), 8.42 (d,J=2.1 Hz, 1H), 8.31 (d, J=2.1 Hz, 1H), 8.00 (d, J=9.0 Hz, 1H), 7.79 (d,J=9.0 Hz, 1H), 7.69 (d, J=16.2 Hz, 1H), 7.04 (d, J=7.2 Hz, 1H), 6.99 (d,J=16.2 Hz, 1H), 6.37 (d, J=7.2 Hz, 1H), 4.78 (br s, 1H), 3.41-3.37 (m,2H), 2.80-2.58 (m, 6H), 1.93-1.85 (m, 2H), 1.81-1.69 (m, 4H). ¹⁹F NMR(282 MHz, CDCl₃, 23° C., δ): −62.8 (s, 3F).

(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(7-(trifluoromethyl)quinolin-3-yl)hept-1-en-3-ol

Under nitrogen, to(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(7-(trifluoromethyl)quinolin-3-yl)hept-1-en-3-one(705 mg, 1.60 mmol, 1.00 equiv) in THF (16 mL) at 0° C. was added LiAlH₄(1.0 M in THF, 1.60 mL, 1.60 mmol, 1.00 equiv). After stirring for 10min at 0° C., H₂O (54 μL), 15% NaOH aq (54 μL) and H₂O (162 μL) wereadded sequentially to the reaction mixture. The reaction mixture waswarmed to 23° C. and filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography on silica gel eluting with CH₂Cl₂/MeOH to afford 515 mgof the title compound (73% yield).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 9.08 (d, J=2.4 Hz, 1H), 8.37 (d,J=2.1 Hz, 1H), 8.08 (d, J=2.1 Hz, 1H), 7.91 (d, J=9.0 Hz, 1H), 7.71 (d,J=9.0 Hz, 1H), 7.06 (d, J=7.2 Hz, 1H), 6.79 (d, J=16.2 Hz, 1H), 6.53(dd, J=16.2 Hz, 4.5 Hz, 1H), 6.34 (d, J=7.2 Hz, 1H), 4.89 (br s, 1H),4.48-4.40 (m, 1H), 3.43-3.37 (m, 2H), 2.75-2.57 (m, 4H), 1.97-1.42 (m,8H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −62.6 (s, 3F).

9-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-3-(7-(trifluoromethyl)quinolin-3-yl)nonanoicacid (Compound A7)

Under nitrogen, to(E)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)-1-(7-(trifluoromethyl)quinolin-3-yl)hept-1-en-3-ol(515 mg, 1.17 mmol, 1.00 equiv) in MeC(OEt)₃ (12 mL) at 23° C. was addedEtCO₂H (87.3 4, 1.17 mmol, 1.00 equiv). After stirring for 2 hr at 140°C., the reaction mixture was directly loaded on silica gel and purifiedby column chromatography on silica gel eluting with hexanes/EtOAc toafford a crude rearrangement product, which was used in the next stepwithout further purification.

Under air, to the above obtained residue in MeOH-TFA (10 mL-1 mL) at 23°C. was added 10% Pd/C 66.6 mg, 0.0626 mmol, 5.35 mol %) and H₂ wasintroduced with a balloon. After stirring for 1 hr at 23° C., thereaction mixture was filtered through a pad of CELITE®. The filtrate wasconcentrated in vacuo to afford a crude olefin reduction product, whichwas used in the next step without further purification.

Under air, to the above obtained residue in MeOH (10 mL) at 23° C. wasadded 15% NaOH aq (4.4 mL). After stirring for 20 min at 60° C., thereaction mixture was neutralized with 3N HCl and concentrated in vacuoto remove MeOH. The residual aqueous solution was extracted with EtOAc(3×10 mL) and the combined organic phases were washed with NaHCO₃ aq(2×5 mL) and dried (MgSO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography on silica gel elutingwith CH₂Cl₂/MeOH to afford 300 mg of the title compound (53% yield over3 steps).

¹H NMR (300 MHz, CDCl₃, 23° C., δ): 8.93 (s, 1H), 8.40 (s, 1H), 8.03 (s,1H), 7.91 (d, J=9.0 Hz, 1H), 7.70 (d, J=9.0 Hz, 1H), 7.24 (d, J=7.2 Hz,1H), 6.23 (d, J=7.2 Hz, 1H), 3.48-3.40 (m, 3H), 2.80-2.59 (m, 4H),1.95-1.20 (m, 14H). ¹⁹F NMR (282 MHz, CDCl₃, 23° C., δ): −62.7 (s, 3F).

Example 8 Synthesis of(S)-3-(6-(difluoromethoxy)pyridin-3-yl)-3-(2-oxo-3-((3-((5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)methyl)oxetan-3-yl)methyl)imidazolidin-1-yl)propanoicacid

The synthetic route is the same as Example 1 except for substituting atStep-8:(3-((5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)methyl)oxetan-3-yl)methanaminefor compound 6b and continuing the synthetic scheme using the samereaction conditions.

Example 9 Synthesis of(S)-3-(3-(2,2-difluoro-3-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl)-2-oxoimidazolidin-1-yl)-3-(6-(difluoromethoxy)pyridin-3-yl)propanoicacid

The synthetic route is the same as Example 1 except for substituting atStep-8:2,2-difluoro-3-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)propan-1-aminefor compound 6b and continuing the synthetic scheme using the samereaction conditions.

The synthesis of2,2-difluoro-3-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)propan-1-amineis performed as shown in Scheme 3.

Example 10 Synthesis of(S)-3-(3-(2,2-difluoro-3-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)propyl)-2-oxoimidazolidin-1-yl)-3-(6-methoxypyridin-3-yl)propanoic acid

The synthetic scheme is the same as Example 9, except the synthesis inStep 1 uses sodium 2-chloroacetate instead of sodium2-chloro-2,2-difluoroacetate. The synthesis proceeds under the sameconditions as Example 3.

Example 10-1 Scheme 3

The preparation of intermediates C and E is detailed in the literatureand is depicted above (for C; WO2011150156 and for E; Seebach, D. etal., Liebigs Ann. Chem., 1994, 701-717). The formation of the dianion ofE has been described, and it was used to displace substituted benzylicchlorides (Bradshaw, B. et al., Org. Biomol. Chem., 2008, 6:2138-2157.).This event similarly affords complex dithiane F. Fluorodesulfurizationof thioketals has been described with several reagents (Sondej, S. C. etal., J. Org. Chem., 1986, 51:3508-13.); intermediate G is reduced anddeprotected as described in the literature (US20040038963). Fragment His inserted into the known route to produce the target compounds.

Example 11 Testing of the Compounds of Present Invention in CellAdhesion Assays

The ability of compounds to block adhesion of three primary cellcultures: human dermal microvascular endothelial (HMVEC), rat lungmicrovascular endothelial (RLMVEC), and rabbit aortic endothelial (RAEC)cells, to vitronectin coated plates was determined using the followingprocedure. This test demonstrates inhibition of the interaction of αvintegrin on the cell surface with the ligand, vitronectin.

Adhesion plates preparation. 96-well plates were coated with vitronectinin PBS, pH7.4 by incubating 50 μL of the solution (10 μg/ml) for 1.5 hat room temperature or overnight at 4° C. The plates then were blockedwith 1% BSA in PBS (30 min at room temperature) and washed with PBS.

Cell culturing and loading. HMVEC cells (passages (p)9-14) (from Lonza,Allendale, N.J.) RLMVEC cells (p4-14) (from Vec Technology, Rensselaer,N.Y.) and RAEC cells (p4-14) (from CellBiologics, Chicago, Ill.) wereused for the compound testing. Cells were grown in T175 tissue cultureflasks and dislodged by gentle 3 min treatment with Accutase (LifeTechnologies). After washing, the cells in suspension in RPMI-1640 (LifeTechnologies) were loaded with calcein-AM (5 μM) (Life Technologies) for30 min at 37° C. and re-suspended into RPMI w/o phenol red mediumcontaining 10% FBS.

Adhesion assay. The cell suspension was aliquoted into the wells at adensity of 1.0×10⁵ cells/well (RLMVEC) and 5.0×10⁴ (HMVEC, and RAEC).The test compounds are added at the same time with the cells. The platesare incubated for 1.5 h at 37° C. The cells that did not adhere duringthis incubation were removed by gentle washing. The wash was performedby 2 cycles of aspiration of the supernatant and addition of 100 μL ofthe pre-warmed fresh DPBS (Life Technologies). A fluorescence of theremaining cells is measured using multimode plate reader (Victor 2V,PerkinElmer) at an excitation/emission wavelengths of 485/535 nm. Thecompounds were tested starting with maximal concentration of 1 μM withhalf-log dilution schedule. IC₅₀ values were calculated with Prism 5(GraphPad, CA) by fixing the bottom of the curves to a value of blankfor empty wells fluorescence.

As shown in Table 2, all the fluorinated αv antagonists are active ininhibiting cellular adhesion to vitronectin through the αv integrin.Non-fluorinated reference antagonist, L-845704, is shown for comparison.

TABLE 2 Potencies of test compounds to block adhesion of different cellcultures to vitronectin. IC50 (M) Compound # HMVEC RLMVEC RAEC L-8457042.5E−08 5.5E−09 1.0E−08 A1 9.4E−09 3.1E−08 8.4E−09 A2 1.6E−07 6.8E−081.6E−08 A3 6.2E−07 2.3E−07 5.9E−08 A4 4.2E−08 3.2E−08 8.5E−09 A5 2.5E−073.7E−08 2.0E−08 A6 4.4E−08 5.5E−09 4.4E−08 A7 1.3E−07 4.0E−07 2.1E−07

Example 12 Anti-Angiogenic Activity Using Chick Chorioallantoic Membrane(CAM) Assay

CAM surfaces were grafted with gelatin sponges impregnated with theconcentrations of test compounds and 50 ng VEGF dissolved in PBS.Untreated CAM received only VEGF and PBS. Error bars represent SEM, N=5,P values for the treated groups were calculated by comparing with theuntreated group (*p<0.05, **p<0.01, ***p<0.001).

Test Substance Preparation: Test samples and standards were dissolved inPBS and sterilized by passing through a syringe filter (0.22 μm).hVEGF(SIGMA) 50 ng/μl was prepared in sterile PBS.

Grafting: Gelatin sponge (Abogel) was cut in approximately 2 mm³ piecesand loaded with required test substance or PBS and VEGF. The graft wasplaced on the CAM.

Eggs: Fertile hen eggs were procured from a hatchery and were cleanedand decontaminated using alcohol. 1 ml of albumin was removed using asyringe and incubated for 8 days. Grafts were placed on developing CAMsand further incubated to day 12. On day 12, CAMs were fixed with 4%formaldehyde in PBS, dissected and imaged.

Imaging: Fixed CAMs were imaged under constant illumination andmagnification under a stereomicroscope fitted with a digital camera(CANON).

Image analysis: Images were analyzed on MS PowerPoint keeping the imagesize constant. A ring was drawn around the graft and the size was keptconstant. Blood vessels crossing the ring were counted for each testgroup.

Statistical Analysis: Data were analyzed on MSExcel 2007.

As shown in FIG. 1, Compounds A1 and A2 each shows anti-angiogenicactivity in the chick CAM assay, and significantly decreases the numberof blood vessels, as compared to the untreated control.

Example 13 Distribution in Plasma, Aqueous Humor, Vitreous Humor, andRetina After Topical Ocular Administration in Dutch Belted Rabbits

The plasma concentrations and ocular distribution (aqueous humor,vitreous humor, and retina) of Compounds A1, A2, and A3 were determinedfollowing topical ocular administration in Dutch Belted rabbits. Thetest compounds were administered in each eye at a volume of 50 μL/eye ata concentration of 1.0-2.5 mg/mL (compound A2, 1.0 mg/mL; compounds A1and A3 at 2.5 mg/mL). Plasma and different ocular tissue samples werecollected at pre-determined time points (1.0 and 8.0 hours for compoundA1; 0.5 and 8 hours for compounds A2 and A3). Aqueous humor, vitreoushumor, and retina were collected from each eye at each time pointpost-dose. Also, weights were recorded. Plasma and ocular sampleconcentrations of the compounds were determined by LC-MS/MS.

Animal Dosing: The exposure of compounds A1, A2, and A3 was evaluated inDutch Belted rabbits. The study was not blinded. Each compound was dosedas n=3/time point for a total of nine rabbits. Rabbits were housed oneper cage. Animals were not fasted, and food and water were supplied adlibitum.

Animals were anesthetized following the 13IA5 IACUC protocol for thedosing. Each rabbit received a bolus dose of test formulation viatopical ocular administration into both eyes at time zero on the day ofdosing. Plasma and ocular samples were collected at pre-determined timepoints. Animals for the 30-minute and 1-hour time points wereanesthetized for the entire duration of the study. The animals for the8-hour time point were recovered after dosing and then euthanized forsampling purposes.

At each time point, approximately 0.5 mL of blood was collected andplaced into chilled Na-heparin tubes containing citric acid. Bloodsamples were centrifuged at a speed of 3,000 g for 5 minutes to obtainplasma as quickly as possible. Samples were stored frozen at −80° C.until analysis. Animals were euthanized per the 13IA5 IACUC protocol andboth eyes were enucleated immediately. Following enucleation, each eyewas rinsed with PBS. Ocular samples from both eyes of each animal werecollected and weights were recorded. All the samples were frozenimmediately on dry ice, and stored at −60 to −80° C. for analysis.

Analysis of Plasma and Ocular Samples: An LC-MS/MS method was developedfor the determination of Compounds A1, A2, and A3 in rabbit plasma andocular samples. A pre-study standard curve was analyzed to determine thespecificity, range, and lower limit of quantitation of the method.

As shown in FIGS. 2, 3, and 4, Compounds A1, A2, and A3 are eachefficiently distributed to the retina.

The following examples of ophthalmic formulations are given by way ofillustration:

Example 14 Ophthalmic Formulation of Compound A1

Solution Composition I II III Compound A1 2.5 g 2.0 1.0 β-cyclodextrinsulfobutyl ether 10 g 10 g 5 g Boric acid 1.05 g 1.05 g 1.05 g Disodiumtetraborate 0.285 g 0.285 g 0.285 g Sodium Chloride 0.25 g 0.25 g 0.25 gEdetate disodium 2.5 mg 2.5 mg 2.5 mg Propylaminopropyl biguanide 0.03mg 0.03 mg 0.03 mg Water for injection q.s. 100 ml 100 ml 100 ml

The active compounds were added to a solution of borate buffered salinecontaining the β-cyclodextrin sulfobutyl ether, edetate disodium, andpropylamino biguanidate dissolved in sterile water for injection in atared sterile vessel. The pH of the solution was adjusted to 7.5 by theaddition of hydrochloric acid. The composition is sterilized byfiltration through a 0.45 micron filter.

Example 15 Ophthalmic Formulation of Compound A1

Solution Composition I II III Compound A1 2.5 g 2.0 1.0 Hyrdoxypropylβ-cyclodextrin 10 g 10 g 5 g Boric acid 1.05 g 1.05 g 1.05 g Disodiumtetraborate 0.285 g 0.285 g 0.285 g Sodium Chloride 0.25 g 0.25 g 0.25 gEdetate disodium 2.5 mg 2.5 mg 2.5 mg Propylaminopropyl biguanide 0.03mg 0.03 mg 0.03 mg Water for injection q.s. 100 ml 100 ml 100 ml

The active compounds were added to a solution of borate buffered salinecontaining the hydroxylpropyl-β-cyclodextrin, edetate disodium, andpropylamino biguanidate dissolved in sterile water for injection in atared sterile vessel. The pH of the solution was adjusted to 7.5 by theaddition of hydrochloric acid. The composition is sterilized byfiltration through a 0.45 micron filter.

Example 16 Ophthalmic Formulation of Compound A2

Solution Composition I II III Compound A2 2.0 g 1.5 1.0 β-cyclodextrinsulfobutyl ether 10 g 10 g 5 g Boric acid 1.05 g 1.05 g 1.05 g Disodiumtetraborate 0.285 g 0.285 g 0.285 g Sodium Chloride 0.25 g 0.25 g 0.25 gEdetate disodium 2.5 mg 2.5 mg 2.5 mg Propylaminopropyl biguanide 0.03mg 0.03 mg 0.03 mg Water for injection q.s. 100 ml 100 ml 100 ml

The active compounds were added to a solution of borate buffered salinecontaining the β-cyclodextrin sulfobutyl ether, edetate disodium, andpropylamino biguanidate dissolved in sterile water for injection in atared sterile vessel. The pH of the solution was adjusted to 7.5 by theaddition of hydrochloric acid. The composition is sterilized byfiltration through a 0.45 micron filter.

Example 17 Ophthalmic Formulation of Compound A3

Solution Composition I II III Compound A3 2.5 g 2.0 1.0 β-cyclodextrinsulfobutyl ether 10 g 10 g 5 g Boric acid 1.05 g 1.05 g 1.05 g Disodiumtetraborate 0.285 g 0.285 g 0.285 g Sodium Chloride 0.25 g 0.25 g 0.25 gEdetate disodium 2.5 mg 2.5 mg 2.5 mg Propylaminopropyl biguanide 0.03mg 0.03 mg 0.03 mg Water for injection q.s. 100 ml 100 ml 100 ml

The active compounds were added to a solution of borate buffered salinecontaining the β-cyclodextrin sulfobutyl ether, edetate disodium, andpropylamino biguanidate dissolved in sterile water for injection in atared sterile vessel. The pH of the solution was adjusted to 7.5 by theaddition of hydrochloric acid. The composition is sterilized byfiltration through a 0.45 micron filter.

Example 18 Evaluation of the Safety and Efficacy of Topically AppliedTest Compounds in the Laser-Induced Choroidal Neovascularization (CNV)Model in Dutch Belted Rabbits

Healthy male animals weighing between 1.5 and 2.0 kg were used in thesestudies. Animals were weighed prior to dosing and at euthanasia, andmore often if needed. Baseline fundus photography and fluoresceinangiography was performed on each animal prior to CNV induction.

Animals were anesthetized with an intramuscular injection of ketaminehydrochloride (20 mg/kg) and xylazine (2 mg/kg) for CNV induction,fundus photography, fluorescein angiography, and intravitreal (IVT)injections. Rabbits were maintained on isoflurane (approximately 1 to3%) in oxygen (approximately 1 to 2 L/min) as necessary. One drop oftopical proparacaine hydrochloride anesthetic (0.5%) was placed in eacheye before procedures. Additional topical ocular anesthesia was utilizedduring the procedure if needed.

CNV was induced by laser photocoagulation treatment. An external diodelaser was applied to the retina using a laser contact lens and a slitlamp biomicroscope. On Day 1, both eyes of each animal underwent laserphotocoagulation treatment using the following laser settings:

Number of Spots: 12-15 spots per eye

Power Range: 50-200 mW

Spot Size: 20-100 μm

Time: 0.05-0.1 seconds

Following laser treatment, 50 μL of a 25-μg/mL VEGF solution (1.25 μgdose) was intravitreally injected into each eye. Daily gross ocularexams were performed throughout the study period.

Clinical ophthalmic exams (slit-lamp biomicroscopy and indirectophthalmoscopy), fundus photography, and fluorescein angiography wereperformed at baseline and then weekly for up to 6 weeks post-induction.Exams were scored using the McDonald-Shadduck Score System. OpticalCoherence Tomography OCT imaging was performed weekly for diagnosticimaging during the exams.

On the last day of the study, blood sampling was performed just prior toadministration of the AM dose and at 2 hours post dosing. Blood sampleswere centrifuged at a speed of 3,000 g for 5 minutes to obtain plasma asquickly as possible. Samples were stored frozen at −80° C. untilanalysis. At the conclusion of the study, animals were euthanized perthe 13C232Q3 IACUC protocol and both eyes enucleated immediately.Following enucleation, each eye was rinsed with phosphate-bufferedsaline. Ocular samples (aqueous humor, vitreous humor retina andchoroid) from both eyes of each animal were collected and weights wererecorded. All the samples were frozen immediately on dry ice, and storedat −60 to −80° C. for analysis.

As shown in FIG. 5, Compound A1 or Compound A2 effectively reducedlaser-induced choroidal neovascularization, as compared to the vehiclecontrol.

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain usingno more than routine experimentation, many equivalents to the specificembodiments and methods described herein. Such equivalents are intendedto be encompassed by the scope of the present invention.

All patents, patent applications, and literature references cited hereinare hereby expressly incorporated by reference.

1. A compound of formula I:

or a pharmaceutically acceptable salt or solvate thereof, wherein: Z is

R and R′ are each independently H or F, or R and R′, together with thecarbon atom to which they are attached, form a 3- or 4-memberedcarbocyclic or heterocyclic ring; Q is

and R₂ and R₃ are each independently H, F, CH₂F, CHF₂, or CF₃, providedthat one of R₂ and R₃ is not H, provided that the compound of formula(I) contains at least one fluorine atom.
 2. The compound of claim 1,wherein R and R′ are each H.
 3. The compound of claim 1, wherein Z is


4. The compound of claim 1, wherein Z is


5. The compound of claim 1, wherein R₂ is F.
 6. The compound of claim 1,wherein R₂ is F and R₃ is H.
 7. The compound of claim 1, wherein R₂ isCH₂F, CHF₂, or CF₃.
 8. The compound of claim 1, wherein R₃ is F.
 9. Thecompound of claim 1, wherein R₃ is F and R₂ is H.
 10. The compound ofclaim 1, wherein R₃ is CH₂F, CHF₂, or CF₃.
 11. The compound of claim 1,wherein R₂ and R₃ are each F.
 12. The compound of claim 1, selected from


13. A method of treating or preventing a disease or condition mediatedby an αv integrin in a subject in need thereof, comprising administeringto the subject a therapeutically effective amount of a compound offormula I:

or a pharmaceutically acceptable salt or solvate thereof, wherein: Z is

R and R′ are each independently H or F, or R and R′, together with thecarbon atom to which they are attached, form a 3- or 4-memberedcarbocyclic or heterocyclic ring; Q is

X is CH or N; Y is CH or N; R₁ is C₁-C₄ alkyl substituted with 1, 2, 3,4, 5, 6, 7, 8, or 9 fluorine atoms, or C₁-C₆ alkoxy substituted with 0,1, 2, 3, 4, 5, 6, or 7 fluorine atoms; and R₂ and R₃ are eachindependently H, F, CH₂F, CHF₂, or CF₃, provided that one of R₂ and R₃is not H, provided that the compound of formula (I) contains at leastone fluorine atom.
 14. The method of claim 13, wherein Q is


15. The method of claim 14, wherein X is N and Y is CH.
 16. The methodof claim 14, wherein X and Y are each CH.
 17. The method of claim 14,wherein X and Y are each N.
 18. The method of claim 13, wherein Q is


19. The method of claim 13, wherein the disease or condition is adisease or condition in which angiogenesis is involved.
 20. The methodof claim 13, wherein the disease is bone resorption, osteoporosis,vascular restenosis, diabetic retinopathy, macular degeneration,atherosclerosis, inflammation, viral disease, tumor growth, ormetastasis.